166/1999 Coll.
LAW
of 13 October. July 1999
about veterinary care and amending certain related laws
(health law)
Modified: 29/2000 Sb.
Change: 154/2000 Sb.
Change: 102/2001 Sb.
Change: 120/2002 Sb.
Change: 76/2002 Coll., 320/2002 Coll.
Change: 131/2003 Coll.
Change: 131/2003 Coll. (part)
Change: 316/2004 Sb.
Change: 444/2005 Sb.
Change: 48/2006 Sb.
Change: 186/2006 Sb.
Change: 124/2008 Coll., 182/2008 Sb.
Change: 298/2009 Sb.
Change: 291/2009 Sb.
Change: 223/2009 Sb.
Change: 227/2009 Sb.
Change: 281/2009 Sb.
Change: 308/2007 Coll. (part)
Change: 308/2007 Sb.
Modified: 18/2012 Coll., 359/2012 Sb.
Change: 279/Sb.
Change: 64/2014 Sb.
Change: 264/2014 Sb.
Change: 139/2014 Sb 250/2014 Sb.
Parliament has passed the following Act of the United States:
PART THE FIRST
VETERINARY CARE
TITLE I OF THE
BASIC PROVISIONS
§ 1
The subject of the edit
This law incorporates the relevant provisions of the European Union ^ 1) and in
following the directly applicable provisions of the European Union (hereinafter referred to as
"the rules of the European Union") ^ 1a) sets out the requirements of the veterinary service (hereinafter
"the veterinary requirements") on the breeding and animal health and animal
products, governs the rights and obligations of natural and legal persons,
system, competence and powers of the authorities in the exercise of State administration
the field of veterinary care, as well as some professional veterinary activities
and their performance.
§ 2
Veterinary care
Veterinary care under this Act includes the
and animal health care) and its protection, in particular prevention and
the spread of diseases transmissible directly or indirectly between animals of susceptible
species (hereinafter referred to as "disease") and other diseases of animals and their
control, protection of human health from diseases transmissible from animals to
man,
(b)), the care of the health of the animal products and feed production and protection
health of people before its damage or threats to animal products,
(c) the territory of the Czech Republic) the protection against the introduction of animal diseases and illnesses
transmissible from animals to humans and disabled prior to the introduction of harmful
animal products and animal feed from abroad,
d) protection of the environment from adverse effects
animal breeding, production and processing of livestock products, as well as
the protection of animals and their produce from the risks of environmental pollution
environment,
e) veterinary sanitation,
f) supervision of compliance with the obligations and requirements to ensure
These tasks of this Act, special legislation ^ 1) and regulations
The European Union ^ 2) (State veterinary supervision).
§ 3
Basic concepts
(1) for the purposes of this Act, means the
and every breeder who) the animal or animals owned or held by, or
entrusted to take care of them, whether for a consideration or free of charge, and even on the
a transitional period,
(b) any construction, economy) or place where it is
of animal or livestock or
held, including an open-air. If it is kept on a holding or
kept more than one herd or more than one group of economic
animals can get sick of the same disease or diseases which can be transmitted from the
animals to humans (hereinafter referred to as "susceptible animals"), each of these herds
or each of these groups separate epidemiological unit which
has the same health status,
(c) the livestock animals) used primarily for breeding, fattening,
work and other economic purposes, in particular cattle, pigs, sheep, goats,
horses, donkeys and their hybrids, poultry, ratites, rabbits, fur
animals, farmed animals, fish and other aquatic animals, bees and
a bee colony,
d) slaughter animals farm animals that are intended for slaughter and
jatečnému processing and whose meat is intended for human consumption,
e) drain pipe concentration of livestock animals of various animal breeders to
designated place and for the intended purpose, in the case of registered animals according to the
plemenářského ^ 8), Act
(f) the Assembly Centre the holding) marketplace or other place
which animals are collected from different holdings, in particular cattle,
pigs, sheep and goats that have been created by a group of animals intended
to send,
g) animals suspected of animal diseases for which the animals are showing up
clinical signs or post-mortem lesions giving rise to suspicion that the
It's about a disease of animals, or animals which are based on the results
the examination must be considered that are suspected of certain animal diseases,
h) animals suspected of suffering from animals which do not show
clinical signs or post-mortem lesions giving rise to suspicion that the
It's about a disease of animals, which, however, can be on the basis of
epidemiological or other information have considered that came directly or
indirectly into contact with its source,
I) quarantine, traffic temporary and locally separated location of animals
animals suspected of being infected or animals suspected of being infected (
"a suspected animals"), in which the carrying out of preventive,
diagnostic, or therapeutic acts to protect against the introduction of, or
the spread of animal diseases,
j) isolation of a temporary separate location of animals before their inclusion in the
or before the transfer of the holding, in which the
carry out preventive and diagnostic tasks, and monitors the health of the
animals,
k) outbreak the farm or other place where one was detected
or more cases of the disease,
l) disease incidence of the disease situation in a particular territory or in a particular
economy,
m) disease incidence and reasons for the possibility of the spread of disease,
n) animal products the raw materials of animal origin, and it's all part of the
the bodies of animals, in particular meat, offal, fat, skin, bones, blood, glands with
internal secretion, horns, antlers, hooves, hooves, wool, fur, feathers, also
milk, eggs, honey and beeswax, as well as products from these raw materials
they are intended for human or animal,
o) healthy animal products animal products
meet the requirements of the health established by this Act,
special legislation, ^ 3) and the regulations of the European Union ^ 3a)
p) feedingstuffs: products of vegetable or animal origin, fresh or
preserved and products of their processing, as well as industrial
organic and inorganic substances, with or without the addition of additives
they add that they are intended for animal feed alone or in
mixtures,
r) healthy feedingstuffs feedingstuffs which meet the requirements of the
wholesomeness established by this Act, special legal
^ 4) rules and regulations of the European Union ^ 4a),
with proprietary veterinary products) products which are
intended for animals, particularly dietary, vitamin, mineral and
cosmetic products, or for a specific laboratory diagnosis
of animal diseases or disease agents from food of animal origin; for
veterinary products are not products subject to special
the legislation of the ^ 5),
t) veterinary technical resources, equipment, instruments, tools,
materials or other items or products, including accessories,
used alone or in combination, together with the necessary programming
equipment that are intended to be used in animals for the purposes of the prevention,
the investigation, diagnosis, monitoring, treatment or alleviation of disease, injury
or disability, replacement or modification of the anatomy
structure or a physiological process or control of pregnancy, and that
do not reach its principal intended action in or on the body of the animal
pharmacological or immunological effect or by influencing the
metabolism, however, whose functions may be supported by such effects; for
Veterinary technical resources to further consider the products that are used
the marking of animals and which are for this purpose vpravovány into the body
of the animal,
u) withdrawal period between the last administration of the medicinal product
animals under normal conditions of use of the relevant product and
at the moment when you can get food from these animals so that
to ensure that such foodstuffs do not contain residues of medicinal products in the
quantities in excess of the maximum limits laid down by a specific legislative
the rules and regulations of the European Union ^ 5a)
in the killing of an animal being slaughtered) in order to use its products,
in a way that does not conflict with the rules on the protection of animals against
cruelty ^ 6)
x) for killing the death of an animal, unless it is a defeat, in a way that
is not in conflict with the rules on the protection of animals against cruelty, ^ 6)
s) veterinary goods animals, animal products, animal feed
origin, other products and articles if they can be carriers of pathogens
diseases,
of) objects that may be carriers of disease agents, live agents of diseases
animals for research or other purposes and objects used in the treatment of
and the transport of animals, animal products and feed, including water, food,
bedding, means of transport, containers, tools, equipment and work
AIDS, or even other objects, if for any other reason may be
carriers of disease agents
AA) putting into circulation, offering for sale, sale or any other form of
menu for consumption, including storage and transport for the needs of sales
or other offers for consumption,
BB) trade trade between Member States of the European Union (hereinafter referred to
"Member State") with animals and animal products originating
in the Member States, as well as with animals and animal products,
originating in countries which are not Member State (hereinafter referred to as "the third
the country "), in the Member States which are in free circulation,
CC) means the part of the road vehicle, the vehicle's overhead,
the aircraft or ship, designed to carry goods, as well as a container that is used
for road, rail, air and water transport,
DD) consignment of a certain quantity of animals of the same species or a certain amount of
animal products of the same type, covered by the same veterinary
the accompanying animal health certificate or other, as appropriate, a commercial document
transported in the same means of transport,
EE) the approval of the consent to the exercise of an activity on the basis of
compliance with the conditions laid down in this Act,
FF) entry in the list of registrations,
Gg) official veterinarian means the veterinarian veterinary
management, the official veterinarian is also considered a veterinary
doctor of Ministry of Defense or Ministry of Interior, where appropriate, by
set up by organisational units of the State, which was entrusted with the tasks of the
coming under this law the official veterinarian,
HH) private veterinarian performing
Veterinary therapeutic and preventive activities of the business way
II) approved veterinarian private veterinarian
approved by the regional Veterinary Administration for a network of epidemiological
performance monitoring and for some, this Act provided for the activities.
JJ) treating veterinarian of the private veterinarian or
the veterinarian Department of Defense engaged in veterinary medical
and preventive activities in the economy or in animal husbandry, which is
He became acquainted with conditions of animals kept or held in this
economy or in this breed.
(2) Where this Act is talking about animals, this means according to the nature of the
things and circumstances whether or not sperm, egg cells, embryos, eggs for hatching,
the fertilized eggs and plemenivo the bees.
(3) where in this Act talks about the game, it is understood for the purpose of
This Act of the body, as well as all of the edible part of the wild
ground game. ^ 7)
(4) Where, in the regulations of the European Union in the context of talking animals of
part of the territory of the State as the region shall mean for the purposes of this Act,
region. ^ 7a)
(5) the management of minor animal products not covered by the law
on waste, except in cases laid down by the EU regulation ^ 7b).
(6) If this Act used in connection with the legal relationships
revised regulations of the European Union concepts whose content and meaning are not
defined in this Act, but in the said legislation, it is for
the purposes of this Act the definition of these concepts in the said legislation.
(7) If this Act is spoken of in the context of the free movement of persons
or to the recognition of professional competence by the Member State, this means
also, the other Contracting State to the agreement on the European economic area, or
The Swiss Confederation.
TITLE II
ANIMAL HEALTH AND ITS PROTECTION
Section 1
The obligations of the breeders
§ 4
(1) the keeper shall be obliged to
and treat animals way) in an environment and conditions that require
their biological needs, physiological function and health status, and
to prevent damage to their health,
(b)) to monitor the health status of the animals, in justified cases in a timely manner
provide first aid and ask for professional veterinary assistance,
c) prevent and the spread of diseases and other diseases of animals and meet
the obligations laid down by law or on the basis of the control
such disease or other diseases of animals ^ 7 c),
(d)) provide the necessary cooperation and assistance in order to be properly
done mandated examination of the animal, sampling, protective vaccination
or other professional health Act, for example, the fixation of the animal,
demonstration of the pet animal,
e) administer to animals only medicinal products subject to prescription
veterinarian, just according to his instructions,
(f)) to ensure that the dogs were, as well as foxes and Badgers kept in captivity,
age from 3 to 6 months to be validly vaccinated against rabies in ^ 7 d), and then during the
the period of effectiveness of a previous vaccine přeočkováni, store
proof of vaccination for the duration of the vaccination and, on request, to
submit the official veterinarian,
g) ensure that it promptly and to the extent strictly necessary for the
the exclusion of the suspicion of rabies veterinary disease examined
animal, human or poranilo with it came into direct contact
manner or in circumstances which may give rise to the suspicion of
that disease, disease
h) comply with the obligations arising from the regulations of the European Union ^ 7 g).
(2) for use in artificial insemination, embryo transfer, and naturally can be used
only animals, which according to the results of the tests meet the conditions laid down
This Act and breeding law ^ 8).
(3) the breeder, who intends to use animals in experiments, ^ 9) is required to
ask the regional health administration of the State Veterinary Administration or
Public health management in Prague, the State Veterinary Administration (hereinafter referred to as
"regional veterinary administration of the determination of the conditions of the veterinary service (hereinafter
"the animal health conditions") for their implementation.
Section 4a
(1) the keeper shall ensure that dogs, cats and ferrets in pet food
breeding, when they are transported within the non-commercial movement between
the Member States or between Member States and territories and third countries
According to the article. in article 13(3). 1 of the European Union concerning animal health conditions
for the non-commercial movement of pet animals ^ 48), meet the conditions
laid down in this regulation.
(2) if it is being transferred more than five animals referred to in paragraph 1,
which do not meet the conditions referred to in article 5 (3). 2 of the European
Union concerning animal health conditions for non-commercial movements of animals in
Pet ^ 48), the breeder must ensure compliance with the requirements
referred to in title IV.
(3) a document that allows you to discover the identity of the animal and its control
health status (hereinafter referred to as "pas") ^ ^ 49), 50), issued by a veterinarian
approved for this activity the regional Veterinary Administration.
(4) an approved veterinarian when issuing and filling in the passport shall proceed
According to the article. 22 European Union legislation concerning animal health conditions for
non-commercial movements of pet animals ^ 48) and is obliged to keep
the records referred to in article 3(1). 22 paragraph 1. 3 of the European Union on veterinary
conditions for non-commercial movements of pet animals ^ 48) for
at least 3 years, to forward these records Chamber of veterinary surgeons of the Czech
Republic of China (hereinafter referred to as the "Chamber") and on request, submit to the official
veterinary surgeon.
(5) the approval of a private veterinarian can be a regional
veterinary services is suspended or withdrawn, if this doctor
issued a passport with demonstrably untrue information, or an incompletely filled
incorrectly, or in violation with the terms of this Act or the
the EU regulation on the animal health requirements applicable to non-commercial
movements of pet animals ^ 48).
(6) records of passports is leading the Chamber. The Chamber will allow the veterinary administration authorities
extract from the register of all the information necessary for the performance of the health
supervision.
(7) the implementing legislation adjusts in more detail the marking of dogs, cats and
ferrets and lays down the method of manufacture, issue, and page numbering
passports, keeping their records, the method and time limits for the transmission of data to the
This evidence, the content of this evidence, requests for the recording of data in the
the passport and its pattern.
§ 4b
(1) the Central Veterinary Administration registers on the basis of a written application
and a person for the purposes of the production of) passports (hereinafter referred to as "the manufacturer of passport") to
the application shall be accompanied by the Passport proposal modelled on the implementing
legal act, and
(b)) a person for the purposes of the distribution of passports (hereinafter referred to as the "distributor of passports").
(2) the manufacturer of passport is required to
and) ensure that the passports corresponded to the model laid down in the implementing
prescription,
(b) the number of passports) allocated by the Central Veterinary Administration series in
accordance with article 6(1). 21, art. 3 of the European Union on veterinary
conditions for non-commercial movements of pet animals ^ 48),
(c) to supply passports only), the distributor of passports,
(d)) to pass a records produced passports Chamber in the manner prescribed
the implementing regulation and to submit to the State upon request
animal health management and
(e) the Central Veterinary Administration) to notify their production of passports.
(3) the Distributor is obliged to passports
and to deliver the passports only) veterinarians approved to issue passports
pursuant to Section 4a,
b) keep records of passport supplied by art. 23 para. 2 CCIP
The European Union on the animal health requirements applicable to non-commercial movements of animals
Pet ^ 48) for at least 3 years,
(c) forward the records delivered) passports according to art. 23 para. 2 CCIP
The European Union on the animal health requirements applicable to non-commercial movements of animals
Pet ^ 48) Chamber of the manner laid down by the implementing
law and upon request, to submit to the State Veterinary Administration and
(d)) to notify the central veterinary administration of their distribution of passports.
§ 5
(1) the keeper of livestock is also required to
and secure implementation of the examination) health examinations and mandatory
preventive and diagnostic operations within the veterinary checks
health, health and control inheritance checks of animal welfare, in
the extent and time limits laid down by the Ministry of agriculture (hereinafter referred to as
"the Ministry") under section 44 para. 1 (b). (d)), keep their results
for at least 1 year and on request to submit the official
veterinary surgeon. If you need to perform also the laboratory examination
samples, this examination must be carried out in the laboratory referred to in § 52
paragraph. 3,
(b)) to the extent appropriate secure species, how they
breeding and lairaging of cleaning, disinfection, disinsectization and meanwhile, the stables,
other spaces and facilities, in which animals are bred, as well as
cleaning and disinfection of equipment, means of transport,
machines, tools, tools, tools, and other objects,
come into direct contact with the animals, use the products
approved in accordance with this Act or special legislation, ^ 9a)
follow the instructions for their use and treat minor animal
products in the manner prescribed by this Act and the regulations of the European Union
^ 9b)
(c) in case of danger) introduction of diseases or diseases transmitted from animals
to establish, where appropriate, to place human resources used to protect the
against the diseases and diseases transmissible from animals to man and care about their
the proper operation,
(d)) of the animals use water that does not jeopardise the health status of the
animals and the wholesomeness of the products, and animal feed
use only wholesome feedingstuffs,
e) administer to animals only medicinal products in accordance with the rules for
their use in providing veterinary care, ^ 5) the animal health
products approved under this Act, of the additive in accordance with the
special legislation ^ 4) and comply with the conditions for the submission of
some of the substances and preparations to animals, whose products are designed to
human consumption (19), to provide the necessary assistance to the authorities
carry out sampling and investigation in connection with the implementation of the plan
monitoring the presence of certain substances and residues thereof in animals, in
animal products, animal feed and drinking water (hereinafter referred to as "plan
the monitoring of certain substances and residues thereof "), and comply with the measures
adopted on the basis of this investigation,
(f) should not be administered to animals) substances and preparations whose use in
farm animals or animals, whose products are designed to
human, is not permitted (section 19 para. 1 and 3) ^ 9 c),
(g) submit on request) the official veterinarian records
laid down special legal regulation 9 d) ^ ^ and allow access to these
also private veterinarian records, issuing the certificate of
State of health of the animal and the health situation in the place of origin (hereinafter referred to as
"medical certificate"),
h) in the case that animals farmed behaves, notify the County
the Veterinary Administration of at least 7 days in advance of their start and end
animal husbandry service activities in relation to farmovému breeding game.
(2) the Breeder, who as an entrepreneur ^ 10) acts for livestock
the purpose of the business, it is also required to
and notify the regional health administration) of at least 7 days in advance of the commencement and
their business activities, as well as to inform the regional
Veterinary Management without undue delay about the changes that will occur in the
how the housing or in the species of animals kept,
(b) the placing on the market) only animals which have not been given unauthorised or
^ 4) prohibited substances or preparations (section 19), keep a record of when and
that medicinal products and substances, which may be adversely affected by the
animal products have been administered to the animals, without delay, submit to the
veterinarian records, noted the Administration
preparations to animals or the vaccination of animals, to keep these records for at least
for 5 years and comply with withdrawal periods,
(c)) to ensure that work in the treatment of the animals and obtain their
products only to persons qualified to carry out such activities in accordance with
specific legislation, ^ 11) that have the basic knowledge about the care of
the animals and the sanitary requirements for the acquisition of livestock products,
d) process and update according to the approved principles [section 44 (1) (a).
c)] a contingency plan in case of the occurrence of dangerous infections and diseases
transmissible from animals to humans, as well as for the case of an emergency
situation (hereinafter referred to as "contingency plan"), and in accordance with national
program control of one or more diseases, diseases transmissible from animals to
humans and agents of these diseases and disease (hereinafter referred to as "the program recovery
animals ') own healing program, submit it for approval to the
the regional Veterinary Administration and follow this program.
(3) the Breeder, who rears poultry as part of their business, it is also
shall immediately after finding a decline in food and water, the decline in
in the production of eggs or poultry increased mortality over the limits set
an implementing regulation to report these facts in the County
the Veterinary Administration.
(4) Implementing law provides
a) animal health requirements for environments in which animals are kept on the
its care and protection from diseases and communicable diseases from
animals to humans and their placing on the market,
(b) substances and preparations) which could not be put into circulation and administered to the animals,
that substances and preparations cannot be administered to animals of certain species and
substances and preparations may be administered to animals of certain species only in certain
terms and conditions and these terms and conditions,
(c) the procedure for processing) of the contingency plans and ozdravovacích
programs of breeders ' point of view, according to which these plans and programmes
process, and what they contain,
(d)), in which cases and under what conditions the State Veterinary
enable management within the limits set by the legal acts of the European Union
mitigate the health requirements laid down in the animal health and their
well-being,
e) limits the downturn in food and water, the decline in egg production
or increased mortality of poultry, above which there are breeders,
who like poultry entrepreneurs for business purposes, required to
to report on these facts the regional Veterinary Administration.
Section 5a
(1) with regard to the rearing of aquaculture animals, the breeder
obliged to further
and the regional health administration) may apply for approval and registration,
where appropriate, only the registration of the aquaculture production business or
Special rybochovného device in which are farmed aquatic animals
(hereinafter referred to as "equipment for the breeding of aquaculture animals"),
notify the regional Veterinary Administration start date for animal husbandry service activities,
run it only after the approval or the registration of, and communicate
the regional veterinary administration of changes to the information provided in the application. In the application
shall indicate the
1. in addition to the information laid down for the submission of the administrative order of the phone number,
fax or e-mail address,
2. the species reared in aquaculture animals, ways
their breeding, water resources and the location of the discharge,
(b) keep a record of the movements of) the aquaculture animals and
products thereof to or from the holding,
in a way that will allow to determine the place of origin and place of destination
relocated creatures, about úhynech animals originating from
aquaculture in each epidemiological unit, and keep logs on
control findings taken from the official controls carried out, after
for at least 2 years of their takeover.
(2) the regional Veterinary Administration and registers,
registers of establishments for rearing of aquaculture animals,
If this device corresponds to its location, the design, the material
veterinary equipment and personnel requirements for such
devices and their operation and its activities does not constitute an unacceptable
the risk of spreading diseases to farms or mollusc farming areas,
or the spread of diseases in the population of aquaculture animals
Wild in the vicinity of the farm or mollusc farming area.
Before any must, however, not accepting regional animal health management in
the applicant's suggestion to consider possible measures to mitigate the risk, including the possible
an alternative location for the device.
(3) if the regional veterinary services finds that are not being met
the obligations of the breeder or the rules for breeding animals originating from
aquaculture, provided for in this law, the approval and registration
suspend or withdraw.
(4) Implementing law provides
and content requirements) the request for approval and registration, or just about
registration of establishments for rearing of aquaculture animals,
the method and timing of notification of changes to the data referred to in the request,
(b)) that establishments for rearing of aquaculture animals may
only be registered,
(c)) the animal and public health requirements for animals originating from
aquaculture and breeding, to the marketing of animals originating in
aquaculture and products thereof on the market and to discharge freely
wild aquatic animals to a facility for animal breeding
of aquaculture,
(d) the keeping of lists) way of authorised and registered,
registered establishments for rearing of aquaculture animals
and the farmers ' records referred to in paragraph 1 (b). (b)).
Section 2
Relocation and national transport of animals
§ 6
(1) If this Act or the regulations of the European Union, unless otherwise specified
the breeder from which the animal is moved within the community, shall be obliged to request a
veterinary certificate to the transfer
and the Assembly Centre), or
b) test animal, unless it is an animal from a breeding or
the upstream device ^ 6), or
c) outside the region of hives ^ 7a).
(2) the animal health certificate must be requested also to relocate the animal in the
within the protection zone or the surveillance zone, where applicable, the additional bandwidth with
restrictions, or even outside of this zone, where the transfer of the animal occurs
on the basis of the emergency veterinary measures in cases in which
This law or the regulations of the European Union allow you to permit exceptions from the
the ban on the movement of animals.
(3) the health certificate to transfer the marketing of the animal shall be issued
only if the animal made the required
medical tests or vaccinations and conditions referred to in § 5 para.
1 (b). and if it is), and this animal is marked and registered in accordance with
plemenářského law ^ 9 d). The breeder from which the animal is moved within the community, it is
obliged to pass a copy of the results of such examinations or vaccination details
dairy farmer or operator, to whose economy or
the animal is moved within the Assembly Centre.
(4) a transfer of the animal health certificate must accompany the animal to
to the place of destination and must be kept at least keeper for 1 year
from the day of its release.
(5) the time limit for the submission of applications for the issue of a health certificate to the
the transfer of the animal shall be at least
a) 2 business days prior to the date of the intended transfer of the animal, if it is
of the animal in which the medical tests have been carried out or vaccination
referred to in paragraph 3, or
(b)) 14 days before the date of the intended transfer of the animal in the other
cases.
(6) unless otherwise provided, the period of validity of the veterinary
72 hours of its certificate issuance. However, the regional Veterinary Administration
may, where justified, provide for a different period of validity
the veterinary certificate and indicate it in it.
(7) in the case of the transfer of the animal referred to in paragraph 1, the farmer's
request before submitting an application for the issue of a health certificate
also, the medical certificate issued by a private veterinarian; It
does not apply to the movement of beehives. A private veterinarian who
issued a medical certificate is required to keep a copy of it for 3
years of age.
(8) the implementing legislation provides for
and conditions of the issuing of the health certificate) and the certificate of health
the transfer of the animal and their content requirements,
(b)) animal health requirements for the location and the keeping of animals in isolation, including
determination of professional veterinary operations, which are carried out in
connection with the location and the holding of animals in isolation,
(c)) in which cases and under what conditions can the regional veterinary
enable management in accordance with legal acts of the European Union to soften the
exceptions to the veterinary requirements for the movement of animals between Member
States, in the case of temporary relocation for grazing or for use to
sporting, cultural or other similar purposes.
§ 7
(1) the collection of animals to be transported, their loading, transhipment and
unloading is carried out under the supervision of the keeper or its designee.
The places where the animals are collected, loaded, translated and
interpreted, must meet the requirements for the protection of the health and welfare of animals
and be regularly cleaned and disinfected.
(2) animals may be carried only under the conditions laid down in this
by law, the law on the protection of animals against cruelty ^ 6) and legislation of the European
Union governing the protection of animals during transport of ^ 14); the official veterinary
doctors shall keep to compliance with these terms.
(3) the transport of animals may be used only to transport equipment,
that
and its design), the design and equipment requirements
the transport of animals of the species concerned, do not damage their health, does not
pain and suffering to them, preventing them from escaping or falling out and protect them
against adverse weather conditions,
(b)) are secured against loss or water flow, feed,
bedding, excrement and other waste,
(c)) have been before and after the cleaned and disinfected,
(d) additional requirements) are laid down by the law on the protection of animals
against cruelty ^ 6) and European Union regulations governing the protection of animals
during the transport of ^ 14).
§ 8
(1) the carrier who holds an authorization to transport cattle, swine,
ovine or caprine animals, issued by the regional veterinary services under this Act
and European Union legislation governing the protection of animals during
transport of ^ 14) is required to
and) have available appropriate facilities for the cleaning and disinfection of the transport
the funds, approved by the regional veterinary services, including
(the device) for storing litter and dung, or submit to the County
the Veterinary Administration of proof that these operations are carried out for it by another
person authorised by the competent authority,
(b) the transport of animals) to use means of transport that were immediately after the
each shipment of animals or products which might affect the health
animals, and if necessary before any new loading of animals,
cleaned and disinfected with disinfectants registered and
procedures or medicines, whose entry into circulation were allowed ^ 5),
(c)) to ensure that the animals being transported is accompanied by the required
the accompanying documents,
(d)) to ensure that transported the animals coming during transport at the time of
between leaving the holdings or the Assembly Centre of origin and
arriving at destination come into contact with animals of a lower health
status,
e) lead for each vehicle used for the transport of animals, records of
carried out by the transport and the cleaning and disinfecting vehicles and put in them
1. place, date and time of receipt of animals to be transported,
2. first and last name or business name and address of the holding or
the Assembly Centre where the animals were taken,
3. expected time of transport,
4. place, date and time of delivery of animals transported,
5. first and last name or business name and address of the beneficiary or beneficiaries
of animals transported,
6. the species and number of animals being transported,
7. data on the accompanying documents, including their numbers,
8. date and place of the cleaning and disinfection of vehicles,
(f)) to keep a record referred to in (e)) for at least 3 years and at the
request, submit to the official veterinarian.
(2) the provisions of paragraph 1 shall not apply to a carrier carrying cattle
or pigs to a maximum distance of 65 km counted from the place of departure
to the place of destination.
(3) a person who operates a slaughterhouse, a place designated for the regular holding of
the lure of the animal or other place to which they are regularly transported
animals, is obliged to create conditions to ensure that after completion of the transportations
the animals could perform the cleaning and disinfecting of the carrier of the vehicle used in the
its device.
(4) in the case of transport of aquaculture animals, the
the carrier shall be obliged to keep records of the úhynech of those animals during the
the transport, if this is possible due to the nature of these shall
animals on farms, mollusc farming areas and
processing establishments visited by means of transport and the
water exchange during transport, in particular the sources of water and places its
the discharge.
(5) the implementing legislation shall determine the method and procedures for cleaning and
disinfection of means of transport used for the carriage of animals, the requirements
the area intended for the cleaning and disinfecting of means of transport,
as well as additional requirements on the prevention of diseases and their spread
the transport of animals.
§ 9
Lead animal
(1) Lead the animals may be just under veterinary supervision.
(2) the organizer of the Assembly is required to ask a municipality for authorization of the venue
Assembly.
(3) the organiser downspout is also required to request prior to the application
referred to in paragraph 2 from the regional veterinary administration of animal health conditions for
the holding of the Assembly and to ensure their compliance.
(4) the regional Veterinary Administration registers circuses, publishes the indexes
animals in the circus ("circus animals") and the registers of locations
performances of the circus and carry out other tasks arising for the official
veterinarians from the European Union on veterinary legislation
requirements for the movement of circus animals between Member States ^ 14a).
The animal health conditions laid down in European Union regulations governing
animal health requirements for the movement of circus animals between Member
States ^ 14a) for the movement of circus animals between Member States,
apply to the national movement of such animals.
(5) the Passports for circus animals exhibit the approval of veterinarians
for this activity [§ 3 paragraph 1 (b) (ii))] and confirmed by an official veterinary
doctors of the respective regional veterinary administrations; Register of such passports
leading the Chamber. The approval of the veterinary surgeon for this activity can be
suspended or withdrawn the veterinarian who issued the passport with
demonstrably untrue information, filled incorrectly or incompletely or
in accordance with the conditions laid down by the legislation of the European Union governing the
animal health requirements for the movement of circus animals between Member
States ^ 14a).
§ 9a
Assembly Centre
(1) the Assembly Centre must
and) be
1. arranged and equipped in a manner consistent with the purpose of the Assembly
the Centre, including facilities for the performance of the State veterinary supervision,
2. cleaned and disinfected prior to use according to the instructions of the official
veterinarian,
3. placed at a time when the animals are collected, in the area of
not subject to extraordinary health measures applicable to
animals of the species concerned,
b) admit only animals that are identified and registered in accordance with
plemenářského law ^ 9 d) and accompanied by a health certificate and that
When coming to the Assembly Centre supervised by an official
veterinarian or approved veterinarian,
(c)) ensure appropriate care and well-being of the animals,
(d)) have a sufficient number of veterinary surgeons approved for
Assembly Centre,
e) comply with the obligations and requirements set out for muster
the Centre of this Act and the regulations governing the protection of the European Union
animals during transport ^ 14)
(f)) be subject to state veterinary supervision.
(2) the operator of an Assembly Centre shall keep, for a period of
at least 3 years to store and, on request, provide the official veterinarian
the doctor records of the data concerning the adopted animals and their
breeders, the places of their origin, and the implied locations, to which they are
sent, carriers and means of transport, which bring the animals into the
the Centre and carried them from the Centre.
(3) the Assembly Centre must be approved and registered with the
the veterinary services; such approval may be limited to a certain kind of
animals for breeding and production or to animals for slaughter.
The regional Veterinary Administration and registers the Assembly
Center that its design, material and personnel equipment
the purpose of the Centre and animal health requirements on them, and shall allocate to
Veterinary approval number. If the regional animal health management
It finds that the operator's obligations are not being met at the Assembly
the Centre, or rules for the operation of the Centre provided for in this Act,
It is entitled to suspend or withdraw the approval.
(4) the regional Veterinary Administration inspects for the approval of veterinary
doctor Assembly Centre, whether this veterinarian has
financial interest in the Assembly Centre and that are not
operator of the Assembly Centre persons each other loved ones.
May decide to suspend approval for the activity of the Assembly
Centre of the private veterinarian, if the veterinary
the doctor has met the obligations or does not meet the requirements of the veterinary
doctor Assembly Centre and in its activities, laid down in this
Act or the regulations of the European Union, or may decide to withdraw
approval for the activity of the Assembly Center to a private
veterinarian, if the veterinarian repeatedly fail to comply with
obligations or does not meet the requirements for the veterinarian
Assembly Centre and in its activities, established by this Act
or the regulations of the European Union.
(5) Implementing law provides
and arrangement of the material and) personal equipment Assembly
the Centre,
(b)) animal health requirements for the animals to be taken to the Assembly
the Centre,
(c) the request for approval) the details of the Assembly Centre,
d) data recorded by the operator Assembly Centre.
§ 9b
(1) a person who as an entrepreneur ^ 10) directly or indirectly buys and
sold cattle, pigs, sheep and goats for profit, has a turnover
these animals, which will sell again within 30 days, or is moved from
some spaces to other premises or directly to a slaughterhouse, provided that such
other spaces or the slaughterhouse are not in its possession, and that was for
This activity the regional Veterinary Administration approved and registered
(hereinafter referred to as "Merchant"),
and) may buy and sell only animals which
1. are identified and registered in accordance with the law plemenářského ^ 9 d), and if it is not
unless otherwise provided, accompanied by a health certificate,
2. bovine animals come from herds that are officially free of tuberculosis,
brucellosis and leukosis, and in the case of animals for slaughter, which are officially free of
Tuberculosis and enzootic bovine leukosis, and in the case of nekastrovaného
officially brucellosis-free bovine. The State Veterinary Administration may allow
purchase and sale of designated animals for slaughter, which do not meet the stated
conditions, if these animals are delivered as soon as possible directly to the slaughterhouse,
without passes through buildings or other devices of the trader, and
If it is certain that after arrival at the slaughterhouse and do not come into contact with
other animals and are slaughtered separately,
(b)) shall keep records of data stores, store is
for at least 3 years and on request, submit to the official veterinarian
doctors,
(c)) may, in connection with this business use only
the building, where applicable, other devices, which have been registered for this purpose
the regional Veterinary Administration, satisfy the animal health requirements and are
under veterinary supervision,
(d)) shall, when holding bought the animals in their buildings or other
devices, to ensure these animals due care and well-being and
employ in doing so, people who have a basic knowledge about the care of
animals.
(2) the regional Veterinary Administration shall approve and register a trader who
meets the requirements of paragraph 1, and shall allocate to health
the approval number; If it finds that these requirements are not
complied with, it may suspend or withdraw approval.
(3) Implementing law provides
and the animal health requirements) must correspond to the buildings or other
the equipment used by the trader to hold the purchased animal
(b) the request for approval) the details of the trader,
c) authentication method basic knowledge referred to in paragraph 1 (b).
(d)).
Section 3
Diseases and their control
§ 10
(1) the State Veterinary Administration
and) gets, collects and evaluates the knowledge about the suspected occurrence and
on the occurrence and spread of diseases and diseases transmissible from animals to man,
as well as the knowledge on the occurrence of zoonotic agents,
(b)) takes corresponding measures on communicable diseases, diseases of the
animals to humans and other animal diseases and to prevent their
the dissemination,
(c)) shall exercise supervision of compliance with the prohibition of vaccination against certain
diseases and diseases transmissible from animals to humans and of compliance with the
measures to which the vaccinated animals are subject to, and in cases of importation
animals for which have not yet been established (harmonised) import conditions
at the level of the European Union [section 34 (1) (b))], specifies that the vaccination
prevents the import of animals and animal products,
d) monitors and evaluates the occurrence of vectors in the case of diseases for which the
the transfer is carried out solely in this way; the vector in this
context means any animal belonging to the obratlovcům or off,
that may be mechanical or biological means to transmit and spread the agent of
the disease.
(2) the list of diseases, the occurrence of which must be in accordance with legal acts of the European
Union governing the reporting of diseases and veterinary expenditure ^ 14 d)
reported to the European Commission (hereinafter referred to as "the Commission") and the Member States,
published in the journal of the Department of agriculture. Of the disease, including diseases
transmissible from animals to humans, that are considered unsafe, and
their agents are subject to reporting to the regional veterinary administration of the Central
the Veterinary Administration of the State Veterinary Administration (hereinafter referred to as "the Central
animal health management ") and are listed in annex 2 to this Act.
(3) Implementing law provides
and the method and time limits) reporting of the diseases referred to in paragraph 2, first sentence,
(b)) for that disease, disease transmitted from animals to humans and their
the originator shall be drawn up in accordance with approved policy [section 44 (1) (a).
(c))] contingency plans
(c)) for that disease, disease transmitted from animals to humans and their
the originator shall be drawn up the healing programs
d) according to which aspects are the procedures for recognising herds, economy,
areas or State as being free of diseases, and in this context when requesting
specific animal health conditions and veterinary, or
health guarantees (hereinafter referred to as "special health guarantees")
applied in accordance with the legal acts of the European Union in trade
animals and animal products, how and what aspects of the
procedures for the suspension, withdrawal or renewal of that status,
(e)) of the disease and the disease transmissible from animals to humans, which may not
the animals have been vaccinated, as well as health conditions and rules of vaccination
in cases in which the required nature of the disease or illness portable
from animals to humans, the circumstances of its occurrence and its consequences, the risk
its spread, or other reasons,
(f) negotiate and) measures to prevent the spread of certain dangerous diseases
and diseases transmissible from animals to humans, the method of placing and holding
animals in quarantine and veterinary support tasks that are performed in the
the course,
g) monitoring rules of diseases and diseases transmissible from animals to humans and
zoonotic agents.
§ 11
(1) a person employed by him, the farmer in breeding, transport, Assembly and
sale of animals, as well as other persons who come into contact with
animals, animal products, or their samples, and that due to the
professional qualifications and experience can recognize the signs
to suggest the suspected occurrence of a dangerous disease or disease communicable
from animals to humans, are required to immediately notify the County
the Veterinary Administration or ensure its awareness of this suspicion.
(2) the obligation to declare the persons referred to in paragraph 1 shall cease as soon as the
suspected presence of dangerous diseases, or diseases transmitted from animals to
a man has been reported to the official veterinarian or the private
veterinary surgeon.
(3) for the user class, the owner or lessee of the pond or
Special rybochovného equipment as well as for other actors in
on breeding and hunting game or fish, the provisions of paragraphs 1 and 2
by analogy.
§ 12
(1) the keeper of the animals on which shows symptoms indicating
suspected presence of dangerous diseases, is required to
and to the arrival of) an official veterinarian to ensure that the
1. animals which are susceptible to the disease and leave their
Habitat,
2. the animal products that come from suspect animals, have not been
used, however processed or put into circulation and that they are
stored separately,
3. objects that may be carriers of disease agents, have not been plotted
or exported and used elsewhere,
4. a suspect animals were disinfected,
5. persons who are treating suspected animals come into contact with
other animals and that in areas that serve the farming of the suspect animals
They other person without good reason,
(b)) after the arrival of the official veterinarian, follow their
instructions and lessons.
(2) a private veterinarian who perform their activities found
suspected presence of dangerous diseases,
and investigate suspected animals), as appropriate, of the dead,
premature, stillborn or killed animals (hereinafter referred to as
"carcases"), and if there is a risk of delay, take samples to
laboratory examination,
(b)) shall immediately so inform the regional Veterinary Administration about suspected presence of
dangerous disease
c) provide the necessary lessons including lessons breeders on the obligation
to take the measures referred to in paragraph 1 (b). and) (hereinafter "the urgent
the measures "),
d) if so required by the nature of the dangerous disease or local conditions, it remains
in place to the arrival of the official veterinarian, and monitors the health
status of the animals.
section 13 of the
(1) the regional animal health management, which was informed of the suspicion of
the occurrence of dangerous disease or is encountered when carrying out its tasks,
examines emergency measures carried out by the farmer and without delay, in
accordance with the uniform procedures and methods approved by the institutions of the European
the Union for the diagnosis and control of the disease and with the emergency
plans and orders, as necessary, shall make a special veterinary measures for
to confirm or exclude this suspicion and to protect the
against the possible spread of the disease and to establish arrangements for implementation of these measures,
in particular, the
and investigate suspect animals and) the carcases, as needed
take samples for laboratory examination and carry out other tasks for the
to confirm or exclude the presence of the disease on the holding,
(b) continue to this economy) monitor and initiate the epidemiological inquiry
aimed at identifying the possible origin and source of infection, time of its
It occurs in the economy, the presence and the deployment of its agents and
vectors and determine the next economy, whose position, arrangement or
contacts with the holding where the suspected occurrence of the hazardous
the disease, to justify the suspicion of the occurrence of this disease in these
farms (hereinafter referred to as "contact holding"),
(c)) shall order the keeper
1. possession of animals susceptible to the disease on their housing
locations and separately from animals suspected and disables the movement of animals from the
holding or holdings
2. make an inventory of animals susceptible to the disease, which are in
economy, and the management and continuous updating of an inventory of animals
dead, infected or suspicious,
3. where the nature of the disease and the circumstances of the case, the losers or
killing an animal for diagnostic purposes,
4. restrictions on the handling of animal products, feedingstuffs of animal origin,
objects, materials and substances that may be carriers of the disease agents
(d)) shall determine the method and rules on the use of appropriate means of disinfection
at the entrances and exits of the places in which they are housed animals are susceptible to
the disease, as well as at the entrances and exits and entrances to the holding
and exits of the holding,
(e) instruct farmers in particular) the nature of the disease and its spread, and options
the further treatment with suspicious animals, animal products,
objects, materials and substances that may be carriers of disease agents.
(2) the measures referred to in paragraph 1 may be extended to the extent necessary
to contact holdings.
(3) if so required by the nature of the disease, the risk of its spread, the risk of
the imminent public or animal health, or the risk of serious injury,
or local conditions, the regional Veterinary Administration measures
referred to in paragraph 1 (b). (c)), and (d)) and in paragraph 2 on the ground.
(4) the Breeder is obliged to accept the measures referred to in paragraphs 1
up to 3 and provide the necessary assistance to perform them.
(5) Regional animal health management
and) terminates the measures referred to in paragraphs 1 to 3, if the suspicion of
the occurrence of dangerous diseases have been excluded, or
(b)) shall proceed in accordance with § 15, if the incidence of dangerous diseases
confirmed.
(6) the provisions of paragraphs 1 to 5 shall apply mutatis mutandis to the muster
centres, slaughterhouses and other sites where it is suspected that the occurrence of the
dangerous disease.
§ 14
There is a suspicion of the occurrence of dangerous infections in animals, which is
participating in the Assembly, and unless otherwise the official veterinarian
the executing state veterinary supervision over the drain pipe, is the operator of a downspout
required to ensure that
and suspect animals was located) separately from the other animals,
(b) the Assembly concerned) the animals to leave its premises and to
It must be other animals
c) animal products and objects that may be carriers of pathogens
the diseases have not been formulated or exported from the Assembly areas,
(d)) of the person that came into contact with suspicious animals, based on the
Assembly areas only with the consent of an official veterinarian, and to
they do them in another person without good reason.
Safeguard and control measures
§ 15
(1) If a dangerous disease confirmed or if there is a risk of
its spread, the competent authority shall, in accordance with the uniform procedures and
methods approved by the institutions of the European Union for the diagnosis and control of
the disease and with the emergency plans of the corresponding special
health measures for controlling the disease and its protection
proliferation (hereinafter referred to as "protective and control measures"), in particular
and) the definition of the outbreak and its warning indication
(b)) the establishment of the protection zone and surveillance zone if necessary and more
the restricted zone,
(c)), or the slaughter of the culling animals sick, according to the circumstances and
suspected and susceptible to disease,
(d) an inventory of the holdings) animals of susceptible species in the zones defined in
subparagraph (b)),
(e) the establishment of rules for movement), transportation and investigation of such
animals in the bands referred to in subparagraph (b)), as well as for the handling of products
these animals,
f) disposal, where appropriate, further processing of
animal products,
(g)) the destruction of contaminated feedingstuffs, other contaminated materials and
substances, as well as contaminated equipment that cannot be
disinfected,
h) cleaning, disinfection, disinsectization and meanwhile, premises, facilities and
means of transport, in which animals are kept or transported
sick or suspect animals, and are susceptible to infection,
I) vaccination of animals,
j) ensure that the awareness of the people in the bands referred to in subparagraph (b))
ordered by the disease control measures, trade and
k) in the case of the disease, whose incidence is mandatorily reported to the Commission and the Member
States, ensure that the public authorities referred to in
the standby plan of the region through the operating and information
Centre the integrated rescue system of the region.
(2) in justified cases, on the outbreak of the disease carries out continuous
the State veterinary supervision.
(3) in accordance with paragraph 1, the competent authority shall proceed even if, if it was confirmed
the occurrence of dangerous disease abroad and if there is a risk of the
introduction in the territory of the Czech Republic.
section 16 of the
(1) Safeguard and control measures may be extended in the necessary
the range also to contact holdings.
(2) the animals intended for slaughter or killed in connection with their
conservation and control measures, the subjects that may be carriers of the
disease agents, as well as animal by-products intended for destruction
delete or further processing can be transported, processed
or disposed of in the manner laid down by the regional veterinary only
Administration.
§ 17
(1) the Authority that ordered the protective and control measures, it shall terminate the
the measure, if it is not the legal acts of the European Union, unless otherwise specified, if
and from the losers or killed), or after treatment, or the death of the
of all the animals of susceptible species in the outbreak of the disease and safe disposal
their carcasses, fixed by the observation period has elapsed and during
prevent further disease that disease or there is suspicion of
This disease,
(b)) were the final cleaning, disinfection, disinsection, and disinfestation in
the outbreak of the disease if these measures were ordered, executed by
the instructions and under the supervision of the official veterinarian in a way that
excludes the spread or survival of the causative agents of disease, and from the implementation of these
sufficient time has elapsed, the measures to ensure that the infection has been completely
eliminated,
(c)) was made the appropriate clinical and laboratory examination, if
and that was ordered, with favourable results.
(2) the regional Veterinary Administration may order that in viewing time will be
in an environment in which diseased animals were kept, placed control
an indicator-based animals are susceptible to the disease.
(3) in view of the progress of the fighting and the risk of spreading dangerous disease
the authority referred to in paragraph 1, change or discontinue some of the ordered
protective and control measures even before meeting the conditions referred to in
paragraph 1, if, due to the epidemiological information already
These measures are necessary and there is no risk of spreading the disease.
(4) the regional veterinary services may to a reasoned request from the breeder or
from official duties to enable an individual exemption from the protection and
effective measures, ordered her or other competent authority,
If this does not jeopardise the control of disease or to increase
the danger of its spread.
§ 17a
A network of epidemiological monitoring
(1) the Central Veterinary Administration may impose on all or part of the territory
the State network of epidemiological monitoring in bovine animals and swine (hereinafter referred to as "network
watching "), through which they ensure the management official
the epidemiological classification of holdings, their regular veterinary
checks, collecting epidemiological data and monitor the health
the situation.
(2) Monitoring Network consists of
and the herd, and economy) of the person responsible for them, approved by County
veterinary services for inclusion in the network monitor,
b) veterinarians holding approval pertaining to network
monitoring,
c) State Constitution for veterinary laboratory Diagnostics (hereinafter referred to as
"the State Veterinary institutes) and laboratories referred to in § 52 para. 3,
(d)) of the State Veterinary Administration, official veterinarians performing the
inspection of slaughter animals and meat and official veterinarians responsible
for assembly centres,
e) ^ 8 the central register) and the digital form of the data in the information system
The State Veterinary Administration (hereinafter referred to as "computerised database").
(3) the Central Veterinary Administration keeps a list of holdings that are
included in the network, and monitor approved veterinarians;
fails to fulfil any of the conditions set by the tracking network participants,
the regional Veterinary Administration shall suspend or withdraw his approval.
(4) the farmer whose holding is included in network monitoring
shall be obliged to
and for its economy) to secure the services of an approved veterinarian.
doctor
(b) without delay to the holding) invite the approved veterinarian,
If the suspected dangerous disease or disease communicable
from animals to humans,
c) realize the approved veterinarian of all the animals comings
to the economy and to place these animals before their inclusion into the herd in the
the isolation in which the course is being validated, as appropriate, in the form of the required
tests whether the health status of the holding can be retained.
(5) the veterinary services shall be approved by the regional veterinarian, if the
This veterinarian has no financial interest in the economy
and if they are not close to each other with keeper persons. If required by the
the right functioning of the monitoring network, the regional Veterinary Administration
specify that the approved veterinarian to act only in a certain number of
economy or only in a particular territory.
(6) an approved veterinarian is required to
and regularly update their knowledge) from the area of animal health, which
regarding the particular species of animals, including knowledge of the legislation,
governing the performance of its duties,
(b)) to provide the necessary information and assistance to breeders to was
all steps to preserve the health status of the holding and to the
compliance with the animal health requirements relating to the marking and registration of
animals, reports of dangerous diseases and any other factors
risk in terms of health or welfare, or health,
rapid determination of the causes of death of animals occurred and where to
sent their carcasses, as well as the hygiene conditions of the herd and
production units of the animals,
(c)) to ensure that the animals, including the animals entering the holding and
animals which are the subject of trade, veterinary
requirements relating to identity checks of animals and veterinary
the certificate.
(7) the computerised database shall be conducted so that it could be always
Figure
and) identification numbers of all bovine animals present on the holding or
in the case of groups of pigs the registration number of the holding of origin, or
the herd of origin and the number of the health certificate, as appropriate,
(b)) for each bovine animal starting with the list of all the holdings,
the holding where the animal was born, and in the case of an animal imported
from a third country, the holding from which they were imported, in the case of groups
the registration number of the last pig farm or last herd,
and in the case of animals imported from a third country, the holding of which was
these animals imported,
(c)), additional data which lays down implementing legislation.
(8) the said data shall be kept in the computerised database for a period of 3 years
following from the death of the animal, in the case of bovine animals, or from the performance of
the last record about an animal, in the case of pigs.
(9) the computerised database shall be fully operational no matter whether
the monitoring network has been introduced.
(10) Implementing legislation may provide that, where required under legal acts
The European Union,
and details for the classification of herds), the economy and the people behind them
responsible to the network monitoring,
(b) the approval of veterinary surgeons) details for the economy,
(c)) other data the computerized database (paragraph 7),
d) measures to ensure the health of animals and prevention of the spread of disease in the
If the conditions have not been met network monitoring.
section 17b
Other diseases and their control
There is a suspicion of the presence of other disease, which for the purposes of this
the Act is not considered to be dangerous, or diseases transmitted from animals
the man, who is not a disease regarded as dangerous, or if the
confirmed occurrence of disease or illness, take, or stores
the competent authority shall take measures corresponding to its nature, severity,
the capabilities of its spread and how to control, as well as the local
conditions.
TITLE III
HEALTH SAFETY OF ANIMAL PRODUCTS
Section 1
Basic animal health requirements for animal products
section 18
(1) animal products must
and) conform to the requirements of their production, processing, storage,
transport and marketing, provided by law, special
^ 3) legislation and regulations of the European Union ^ 14 d)
(b)) to be a wholesome and safe in terms of protecting human health and the
animals, in particular it must not be a source of risk spreading diseases and illnesses
transmissible from animals to man,
(c) comply with microbiological criteria) and must not contain residues and
contaminants in quantities based on scientific evaluation
constitute a danger to human health ^ 14e)
(d)) to be, if it is not prescribed by this Act or the regulations of the European Union
otherwise, the specified way bear the health mark,
or, if it is not the use of the health mark provided for,
identification mark ^ 14f).
(2) animal products which are intended for human consumption, it must be
obtained from animals, which
and) meet the animal health requirements for animals of the species concerned as laid down
This Act, special legislation ^) and regulations 14 g
Union ^ 14 d)
b) come from a holding, territory or part of the undertaking of the territory that
limiting or prohibiting the veterinary measures
apply to the animals and their products, and which was adopted by the
the rules laid down by this Act or by a specific legislative
^ Regulations 14 h) due to the presence of foot and mouth disease, classical swine fever
swine, swine vesicular disease, African swine fever, rinderpest,
Newcastle disease, avian influenza or the plague of small ruminants,
or due to the occurrence of diseases in aquatic animals, fish and shellfish,
referred to in the special legislation ^ 14 h)
(c)) have not been slaughtered, in the case of meat and meat products, in business, in which
during the process of slaughter and production animals infected or was present
suspected of being infected as referred to under point (b)), or carcasses
bodies or parts of bodies of animals, until it was suspected
out of the question,
(d)) are in line, in the case of aquatic animals and animals originating from
aquaculture, with the requirements laid down in specific legislation ^ 14i).
(3) the regional Veterinary Administration may, subject to measures for the control of
the diseases referred to in paragraph 2 (a). (b)), allow for a specified
animal health conditions have been manufactured, processed and marketed
animal products intended for human consumption that originate in the territory of the
or part of the territory, subject to a limiting or prohibiting veterinary
the measures referred to in paragraph 2 (a). (b)), but not from the economy,
in which some of the diseases referred to in paragraph 2 (a). (b)),
or which is suspected of the incidence of such diseases.
(4) animal products for which reasonable doubt about compliance with the
obligations or requirements to ensure their health certificate, and
food of animal origin ^ 15) which were for this reason returned from
the business network, may be used or further processed only
the approval of the regional Veterinary Administration and subject to the conditions laid down.
(5) animal-based foods that are wholesome,
be considered as edible, or edible after special arrangements
(treatment) or from the further processing. Food of animal origin
do not comply with the requirements of the health certificate, shall be considered as
inedible.
(6) the implementing legislation
and) lays down the
1. the animal health and public health requirements for special treatment (treatment), and
the use of animal products referred to in paragraph 3 and intended for human
consumption, as well as the food of animal origin applicable after the Special
treatment (treatment) or from the further processing,
2. the method of labelling meat comes from the territory or part of the territory,
referred to in paragraph 3,
3. which animal-based foods are edible and which are
inedible,
(b)) may provide, where required under legal acts of the European Union, details
on the special adjustments (treatments), where applicable, of further processing and
the use of minced meat, meat preparations, meat products, milk
products and egg products.
§ 19
(1) Animals, whose products are intended for human consumption, may be administered
or they only use additives, medicines and more
preparations intended for these animals that have been produced and brought into
circulation in accordance with this Act and special legislation ^ 5).
(2) animals which have been submitted to the additives, medicines and more
products leaving unwanted residues in animal products,
can be used for the acquisition or manufacture of products for feed
people only after the withdrawal period laid down by the manufacturer or an approved
by the competent authority. In the case of medicinal products which have been used in
the case of the nepředpokládaném decision on their registration, or if it is
about unregistered medicinal products for which the protection is not provided
period, animals may be used in this way after at least
and 28 days), in the case of meat from poultry and mammals including fat and offal,
b) 7 days, in the case of milk and eggs,
(c)) stupňodnů, 500 in the case of the meat of the fish, while the number of stupňodnů is
checks by multiplying the average daily temperature of water by the number of days.
(3) additives and medicinal products which have hormonal,
thyreostatický or beta adrenergic effect must not be put into circulation
and administered to the animals referred to in paragraph 1, except where the
laid down in the implementing regulation.
(4) the drug may be administered to animals in feed mixtures
(medicated feedingstuffs); for the production of such mixtures and putting them into
circulation applies specific legislation. ^ 5)
(5) the use of medicinal products in wild game, whose products
they are intended for human consumption is prohibited, except in cases where it is
the user is obliged to secure implementation of mandatory private hunting grounds, preventive and
diagnostic operations within the veterinary checks the health of the wild
game, and that the extent and time limits laid down by the Ministry in accordance with § 44
paragraph. 1 (b). (d)). the user is obliged to keep a hunting license usage data
medicinal products for wild game in the first sentence for
at least 5 years and on request, submit to the official veterinarian
doctors. Data on the use of medicinal products in wild game
include the type and number of animals, for which a medicinal product used,
the territory in which it was used, the name of the medicinal product and the amount of
of the medicinal product, the date of the use of the medicinal product and the withdrawal period
of the medicinal product.
(6) the implementing legislation provides for
and) how the treatment of animals, which have been administered substances and preparations
referred to in paragraph 3, and with their products,
(b) the method of monitoring the presence of unauthorised) or prohibited substances and
products, as well as residues of substances having a pharmacological action, of their
metabolites and of other substances that were in animal products and
that could be harmful to the health of people, animals, animal
products and drinking water, assistance to the fulfilment of this task
provided by the keeper of the animals and the people who produce and process
animal products, and measures to ensure that the health certificate
animal products, adopted on the basis of the results of monitoring.
Veterinary examination of animal products
section 20
(1) any person who puts into circulation the meat or organs of slaughter and other
animals and products thereof for human consumption or for animal feed,
It may do so only after the examination, assessment and labelling of these products
in the manner prescribed by this Act and the regulations of the European Union ^ 15a), in
According to the results of the examination and assessment.
(2) wild game meat must come from animals caught and killed in accordance with the
special legislation ^ 6) ^ 4) and must be in accordance with the Special
^ Law 16) marked in a way that allows its identification.
(3) fish, crustaceans, molluscs, frogs and other animals of the water and
the terrestrial environment and intended for human consumption must be obtained the permissible
the manner of hunting (catches), capture or collect. ^ 17)
(4) unless otherwise provided, can be put into circulation only
and) milk obtained from animals whose health status, how to
breeding and nutrition do not affect adversely the wholesomeness and
that has been treated with mlékárensky, as well as products made from this milk.
Request the production of dairy products from mlékárensky treated milk, however,
does not apply if the approved technological process requires taking into account the
characteristics of the product to be used in its manufacture mlékárensky
the untreated milk; for this purpose, the production of milk products means
How to change the character of this milk,
(b)) eggs which have been prosvícena and manner marked ^ 17a),
c) med that is harmless and comes from clinically healthy
a bee colony.
section 21
(1) unless otherwise provided, shall be slaughtered in a slaughter
the slaughterhouse under the conditions provided for in this law, the special legal
^ 6) rules and regulations of the European Union ^ 17 c)
(2) animals for slaughter with the exception of bovine animals over 24 months of age, horses, asses and
their hybrids can be slaughtered at the holding of the keeper, if
their meat and organs intended only for consumption at home breeders
(home defeat). This meat and organs shall be subject to veterinary examination,
If so provided by the regional Veterinary Administration with regard to the animal health
situation.
(3) the Home slaughter of bovine animals under 24 months or deer from the
breeding of farmed game can only be performed on the holding of the keeper, which
It was the regional veterinary services on the basis of a written application enabled
the implementation of domestic animals of the species listed in the slaughter that holding.
Regional animal health management in the authorisation shall specify the conditions of implementation home
slaughter. Period of validity of the authorisation is issued for 3 years. If the regional
veterinary services finds that the breeder when performing home defeat
progresses in contravention of this Act or the regulations of the European Union or
violates the conditions set by the regional Veterinary Administration, issued by the
to enable breeders to be withdrawn. Each home defeat of these species is
the breeder shall at least 7 days before the implementation of the report of the regional
the Veterinary Administration. Authorization to perform domestic slaughter of deer
from a farmed breeding in holding the breeder is not required if the
breeders of the permit to the slaughter of the deer family game farmed
breeding in the economy. The implementing legislation provides for content
requirements for an application for authorisation of the home slaughter and containment requirements
her reporting.
(4) Animals farmed can be slaughtered at the farm for only
conditions laid down by the legislation of the European Union ^ 17 c). Authorisation is issued
the regional Veterinary Administration breeders on the basis of a written application, which
meets the requirements of the special legal regulation ^ 17ca) and in which
the breeder provide evidence that the conditions laid down by the regulations of the European
Union ^ 17 c).
(5) the regional Veterinary Administration can to defeat large farmed game in the
the holding referred to in paragraph 4 or to the home slaughter of deer from the
breeding of farmed game to kill these animals allow the use of firearms
weapons. Permit is issued on the basis of a written application, to which the
the farmer must
and) demonstrate that the killing of a firearm does
1. the holder of a firearm licence issued under a special legal
prescription ^ 17cb), or
2. the breeder in person or a person who is in the work, or
a similar proportion, if the holder of the arms licence Group (C) issued by the
under special legislation ^ 17cb), and
(b) attach justification to kill) animal firearm.
For the purposes of this provision, a large farmed game means the deer,
mouflons and wild pigs are bred farmed.
(6) the period of validity of the permit issued in accordance with paragraph 5 is 3 years. Time
the validity of the permit may be extended to regional Veterinary Administration
upon written application by the holder of the permit, 3 months ago
the end of the validity period of 3 years, unless the holder of the authorization shall provide evidence that the
conditions under which the authorisation was granted.
(7) a permit issued under paragraph 5 shall cease, if the
have changed the conditions under which it was issued. Change of the conditions referred to in
paragraph 5 is the breeder shall without undue delay notify in writing
the regional Veterinary Administration.
(8) the regional Veterinary Administration may permit issued pursuant to paragraph 4
or 5 withdraw it if any breach of the conditions under which it was
released.
(9) the Breeder, who is the holder of the authorization referred to in paragraph 5, shall be required to
have a sketch of the farm or farms, with an indication
location of shooting and the means to ensure safety in the shooting, a certified
an expert in the field of ballistics; This does not affect the obligations of the holder
arms licence under special legislation ^ 17cb).
(10) the regional Veterinary Administration shall notify the competent service of the police of the Czech
Republic of place and time of use of a firearm to slaughter animals in the
farmed in the economy or to the home slaughter of deer from the
farmed animals.
(11) to the slaughterhouse must be delivered healthy pregnant breeding.
(12) the animals for slaughter shall be subject to compulsory veterinary at the slaughterhouse
examination before slaughter, their meat, organs and other parts after
the losers (inspection of slaughter animals and meat). Examination (examination)
before slaughter and after the slaughter carried out by the official veterinarian,
meets the requirements of the professional qualifications established by regulations of the European
Union ^ 17e). When it proceeds according to the following rules, which also provides
When and in which cases an official veterinarian need not be present
examination (examination), carried out by the official veterinary assistant ^ f).
(13) the Veterinary examination of the carcasses of hunted wild game and wild game meat is
carried out in the manner and to the extent laid down by the legislation of the European Union ^ 17 g).
(14) in the context of the Veterinary examination of animals for slaughter and animals,
susceptible to trichinosis, are investigating their muscle on the presence
trichinosis (Trichinella). If this test is not done by the regional
the veterinary services shall be carried out in the laboratory referred to in § 52
paragraph. 3.
15) Implementing legislation sets out the rules and procedure of the veterinary
investigation and assessment of animal products, the labelling of the
products on the basis of their veterinary diagnosis, as well as veterinary
the conditions for the release of these products on the market, provided that such rules
the procedures and conditions not covered by European Union legislation, and if
their editing these regulations allow.
§ 21a
(1) the regional veterinary services may, in the cases and under the conditions
laid down in the EU regulation, laying down specific
the rules for the organisation of official controls on products of animal origin
intended for human consumption ^ 42), operators of poultry or rabbit
allow slaughterhouse, to certain acts in a guided tour of meat of poultry and
Lagomorphs were performing employees of the operator.
(2) an employee of the operator of poultry or rabbit slaughterhouses
performing certain acts within the inspection of meat from poultry and Lagomorphs is
obliged to report any faults found the official veterinarian
doctors and undergo specialized technical training with a focus on
the implementation of certain operations within the inspection of meat from poultry and Lagomorphs.
(3) an employee of the operator of poultry or rabbit slaughterhouses is
entitled to certain acts in a guided tour of meat of poultry and Lagomorphs
If the specialized professional training, he graduated from the
focus on the implementation of certain operations within the inspection of meat and poultry
Lagomorphs, he passed the final examination and certificate of
eligibility for this activity. Specialized professional training
organised by the College with the veterinary curriculum, which
issued to persons who have undergone this specialist training
training, certificates, which allows them to carry out certain operations in the
a guided tour of meat of poultry and Lagomorphs, and keep a list of these people.
(4) if the regional veterinary services finds that the operator
poultry or rabbit abattoir in contravention of this Act or
the EU regulation laying down specific rules for the
the organisation of official controls on products of animal origin intended for
human consumption ^ 42), authorisation issued to the operator shall be withdrawn.
(5) Implementing law provides
and) the rules and procedure for carrying out certain operations in the framework of the inspection of meat
poultry and Lagomorphs operator poultry or rabbit
slaughterhouses, including the determination of the scope of such operations,
(b)), the content, scope and organization of specialized vocational training
employees of operators of poultry or rabbit slaughterhouses with a focus
on the implementation of certain operations within the inspection of meat and poultry
Lagomorphs, method and organization validation of acquired knowledge, the issue of
the certificate and the maintenance of a list of persons that this specialized training
training completed.
Section 2
Obligations of persons who manufacture, process and circulate
animal products
section 22
(1) persons who as entrepreneurs ^ 10) procure, produce,
processed, packaged, treated, stored, transported, and the circulation of
animal products (hereinafter referred to as "treat animal products")
of the undertaking, establishment, where applicable, other devices, which are under State
veterinary supervision, have, in accordance with the regulations of the European Union ^ 17 g)
the responsibility to ensure that the various stages of the food chain
not to compromise the health safety of animal products. Are
required to
and) in accordance with regulations of the European Union 5 p.m.) to ask the regional ^ veterinary
management for approval and registration, business registration,
race, or other device, notify the regional Veterinary Administration
date of commencement of activities and operate it only after the approval, if appropriate,
registration and notify the regional Veterinary Administration changes
decisive in terms of approval or registration. In the application
shall, in addition to the kinds of productive activities, which they intend to operate, their
name and surname or business name, place of residence or
residence and place of business if different from the place of residence or
the stay, in the case of a natural person, company or business name, registered office,
where appropriate, the location of the branch on the territory of the Czech Republic, if it is
of a legal person. The conditions of approval, conditional approval,
the suspension or withdrawal of approval, are laid down in the provisions of the European
Union ^ 17 h)
(b)) to secure in all stages of production, processing and marketing of livestock
the products into circulation, in order to prevent the spread of diseases and diseases transmissible
from animals to humans, and in view of the nature of the activity and the type of
animal products
1. comply with the animal health and public health requirements for the production, processing and
the marketing of animal products into circulation, as well as technological procedures,
2. apply the principles of good hygiene practices and procedures based on the
hazard analysis and critical control points (HACCP) ^ 17i)
as a precautionary measure to check the health of the raw materials, accessories,
additives and finished products, and use of knowledge
obtained from the manuals of good hygiene practices, and guides for
the application of HACCP principles, approved by the institutions of the European Union, or
processed by professional interest associations ^ 17j)
3. process and comply with the policy, measures to
ensure the production of healthy ingredients and foodstuffs of animal
of origin and their own checks on the hygiene conditions of production, as well as
technical, technological and personnel conditions of sanitation (hereinafter referred to as
"the operating and sanitary regulations"), and provide operational and sanitation regulations
including the appropriate amendments to the approved regional Veterinary Administration,
4. in accordance with the order of using the cleaning regular cleaning,
cleaning, disinfecting and disinsectisation, meanwhile, premises and
the device and use the products approved in accordance with this Act or the
special legislation ^ 5),
5. keep appropriate documentation of the progress and results of the checks of compliance with the
health requirements and principles referred to in points 1 and 2, keep it
for at least 1 year, unless otherwise provided, and submit it to the
the request of the official veterinarian,
c) refer to foodstuffs of animal origin specified way [section 18
paragraph. 1 (b). (d))],
d) employ when dealing with animal products only by persons
eligible for such activities under special legislation ^ 11),
care about their qualifications and professional training and to lead them to the compliance with
hygiene requirements for the production, processing and marketing of livestock
the products into circulation and to compliance with the requirements of personal hygiene,
(e)) to perform consistently custom checks on the hygiene conditions of production
set microbiological criteria, including sampling and
follow-up examination, keep records of the results of such examinations,
keep these records for at least 2 years and on request, together with the
laboratory protocols provide the official veterinarian.
In the case of laboratory tests to confirm health certificate
animal products must be carried out in the laboratory, which was
for the kind of investigation issued an accreditation certificate ^ 17 k),
(f)) to create appropriate conditions for the implementation of professional veterinary acts
required under this Act and the regulations of the European Union ^ 17 d) to
public health inspection of animal products and compliance with
hygiene requirements for the production, processing and marketing of livestock
the products into circulation, provide details of the official veterinarian
the origin of the raw materials from which they are manufactured foods
(g) to provide the necessary assistance to authorities) that perform a subscription
sampling and investigation in connection with the performance of some of the monitoring plan
substances and residues thereof, and comply with the measures taken pursuant to this
the investigation,
h) in the case of an undertaking with a small volume of production [section 24, paragraph 2 (b))],
comply with the established production capacity,
I) in the case of establishments processing animals originating from
aquaculture products, keep records of all consignments of such animals and their
products that come in these devices, or one of them go,
j) in the case of a firm that handles and puts into circulation the honey of different
breeders, ask the regional Veterinary Administration for approval and registration
the undertaking; in the case of a firm that handles and puts into circulation the med
originating exclusively from own breeding of honey bees, apply to register
the enterprise,
k) in the case of an undertaking which treats animal products originating
of the crocodiles, ask the regional Veterinary Administration for approval and
registration of the business.
(2) the implementing legislation
and) lays down the
1. display the details of the request for approval and registration,
on the registration, referred to in paragraph 1 (b). and the method and deadlines), notification of
changes to the data determined in terms of approval, where appropriate, the registration,
2. the manner of keeping the list of approved and registered undertakings, businesses,
where appropriate, other devices and method of keeping records of the operator according to
paragraph 1 (b). I),
3. the animal health and public health requirements for animal products and treatment
with them, as well as to the labelling of their health certificate, if it
European Union regulations allow,
4. content requirements and sanitary regulations and rules of the personal
hygiene of the staff working with animal products,
(b)) may provide, where required under legal acts of the European Union, details
implementing a custom control persons who handle animal
products, as well as the details of the official veterinary checks,
doctors over the safety of animal products.
Article 23 of the
Obligations of the operator of the slaughterhouse
(1) the operator of the slaughterhouse shall further
and) organize and manage their operation in accordance with the provisions of the European
Union ^ 17 l) and with the principles of animal protection from dangerous diseases,
other harmful influences and mutilation with the animal health requirements for the
the wholesomeness of animal products,
(b) receive at the slaughterhouse) only animals for slaughter
1. that are identified and registered in accordance with the law plemenářského ^ 9 d) and
that he be provided with the information provided for regulations of the European Union,
2. to whom were given illegal or prohibited substances or preparations,
3. to whom were given a substance or preparations whose exposure could
be adversely affected by animal products, but for which demonstrably
have passed the prescribed withdrawal periods,
(c)) to ensure that at any time could be the identity of the received
of animals for slaughter and meat, organs and other parts to them, and
up to assess their edibility, or usability,
(d)) in the plant, where there is no continuous veterinary supervision, report of the regional
Veterinary Management of each shipment of animals for slaughter at least 24 hours
prior to its implementation,
e) the official veterinarian shall immediately notify each disease
or suspicion of disease, injury or death of an animal
(f)) to create conditions for inspection of slaughter animals and meat and to provide
free of charge to persons shall carry out necessary substantive, personal and other
assistance, in particular
1. provide such persons a room suitably equipped for their business
with running hot and cold drinking water and jobs on the production
lines,
2. prepare the animals for slaughter, their bodies, meat, organs and other parts of the
a veterinary examination,
3. perform auxiliary tasks required for this examination,
g) draw up and submit for approval the regional Veterinary Administration
operational and sanitation of procedure and a contingency plan.
(2) animals for slaughter taken to a slaughterhouse must not leave the slaughterhouse premises already
without the consent of an official veterinarian. Sick or from illness
suspect animals for slaughter is slaughter in a slaughterhouse or in a slaughterhouse Department
intended for this purpose. With the approval of the regional Veterinary Administration may
to be slaughtered in slaughterhouses and in spaces intended for slaughter of healthy
animals, but time separately.
(3) animals for slaughter, as required by this Act or the regulations
The European Union, must not be slaughtered for human purposes ^ 17 m).
(4) Implementing legislation may provide that, where required under legal acts
The European Union,
details of the preparation) of animals for slaughter to delivery to the slaughterhouse,
dealing with them in a slaughterhouse, and organization of the operation of the slaughterhouse,
(b) the method of slaughtering animals for slaughter), preparation of animals for slaughter, their
the carcases, meat, organs and other parts to the Veterinary examination,
specific disease, other illnesses or other facts, that prevents
the slaughter of animals for slaughter, as well as the technical conditions for the performance of
the State veterinary supervision at the slaughterhouse,
(c) the auxiliary) range of operations carried out by the operator of the slaughterhouse.
section 24
(1) the premises of the undertaking, business, or other device, intended for
treatment of animal products must meet the requirements of this
the law and regulations of the European Union), and in particular the ^ 17n must be designed,
arranged and fitted so as to permit compliance with the obligations and
requirements to ensure the wholesomeness of animal products and
the hygiene conditions of their production, processing and marketing,
as well as to avoid contamination. Must be
and well maintained, clean) and protected from animal disease agents and diseases
transmissible from animals to humans, arthropods, rodents, and other harmful
animals,
b) arranged so that their parts in which there is a risk of infection
or contamination of animal products intended for human and animal health,
they were separated from the parts in which this danger is not, and to
separated departments with different technological processes and climate
terms and conditions,
c) equipped with machines, devices and other objects which are not active
adversely the wholesomeness of animal products and according to the
expertise and experience enable you to reliably monitor whether and
compliance with the obligations, requirements and values laid down in this
the law and regulations of the European Union to ensure that the health certificate
animal products and sanitary conditions, dealing with them.
(2) the implementing legislation shall in accordance with the provisions of the European
Union ^ 17o)
and the animal health and public health requirements) to businesses, factories and other
the device, which is treated with animal products, and technical
terms of their construction, layout and equipment,
(b)) steps and what criteria can the regional veterinary
Customize management without compromising production hygiene veterinary and hygiene
requirements for enterprises, plants and other facilities in which is treated with
animal products, with the aim of
1. allow enterprises, plants and other equipment for more use of
traditional methods at all stages of production, processing or marketing
animal products into circulation,
2. accommodating the needs of enterprises, plants and other equipment located in the
areas with restrictive geographical conditions,
3. to adapt the requirements for the construction, layout and equipment of enterprises,
plants and other facilities,
4. to accommodate the needs of enterprises, plants and other devices with small
volume production,
5. allow enterprises, plants and other equipment the implementation of operational
tests for validation of new approaches to hygiene control,
(c)) that enterprises, factories, and other facilities are considered to be businesses with a small
volume production,
(d)) that businesses, factories and other installations shall be regarded as undertakings
operating retail activities,
e) content requirements for the adaptation of veterinary and
hygiene requirements for some businesses, factories and other equipment in the
which is treated with animal products.
§ 24a
Retail establishments in which meat and produce
meat products intended for direct sale to the consumer at the point of implementation
those activities, subject to the provisions of the European Union governing the
specific hygiene rules for food of animal origin and
organisation of official controls of animal products, in the case of the establishment,
in which the weekly
and cut more than 5) t meat, except poultry and rabbit meat,
(b)) of cutting more than 2 tonnes of meat of poultry or rabbit, or
c) produced more than 7.5 t meat products.
§ 25
Sale of animals and animal products in the markets and in markets, sales
animal products intended for animal feed
(1) in the markets and the markets [§ 46)], where it was relevant
authorities allowed the sale of animals and animal products, you can only sell
healthy animals and wholesome animal products.
(2) the operator of a market or the market referred to in paragraph 1 shall be obliged to
and submit the regional Veterinary Administration) for approval to market order, if
This order was not issued in the form of regulation. Market order must contain the
animal and public health conditions for the handling of animals and sold
animal products, the cleaning and disinfection of premises rules market
or the marketplace, including disposing of animal
products and other waste, and the rules of personal hygiene of persons involved in
sold to the treatment of animals and animal products,
(b)) to keep a record of persons who in the market or sell in the marketplace
animals or animal products, which contains the name, surname and place of
residence or stay, in the case of a natural person, the name and surname,
where applicable, the trade name, place of residence or stay, and instead
the business, if different from the place of residence or stay, in the case of
entrepreneurial natural person, business name or the name, registered office,
where appropriate, the location of the branch on the territory of the Czech Republic, if it is
of a legal person.
(3) a person who operates a seasonal sale of live fish, must comply with the
the requirements established by this Act and the law on the protection of animals against
cruelty ^ 6) and at least 7 days before the start of the sale, notify the County
the Veterinary Administration, when and at which point the sale will be launched and when
will be terminated.
(4) animal products intended for animal feed may be sold in
food stores only in the form of durable, consumer-packaged
and separately stored products.
(5) Implementing law provides
and) health and hygiene rules for the sale of animals and animal
products in the markets and in markets for seasonal selling fish on the
a separate point of sale and for killing, evisceration and other modifications of the fish,
If these activities are part of their sales,
(b)) that the animals can be sold in the markets and in markets,
c) veterinary, health and technical requirements of the market and market place,
where are sold to livestock and livestock products, and their arrangement
and equipment.
Section 3
National transport of animal products
section 26
(1) animal products shall be transported in accordance with the provisions of the European
Union ^ 17 p) means of transport which are constructed and equipped with
so that they are well to clean and protect the transported products before
deterioration, pollution and contamination, as well as in front of the arthropods,
rodents and other harmful animals, and, if necessary, taking account of the
the type of products to maintain the required climatic
conditions until the end of the carriage.
(2) the means of transport intended for the transportation of animal products
must be properly ventilated, regularly cleaned and disinfected.
(3) the carrier who as an entrepreneur ^ 10) transporting animal products,
is obliged to
and) request prior to the establishment of the provincial veterinary administration of
the registration,
(b)) keep records relating to the cleaning and disinfection of means of transport
used for the carriage of livestock products, as well as on the
carriage, retain it for at least 1 year and at the request of her
submit the official veterinarian,
(c) the regional health administration) allow to before registration can
perform a check of means of transport that will be used to
carriage of animal products; This also applies to means of transport
designed for the transport of animal products that are newly assigned to the
operation.
(4) in a single transport space can be transported only animal
products that are consistently assessed in terms of their health
certificate and, where appropriate, satisfactory, of usability, and for which the
There is no mutual negative influence.
section 27 of the
(1) the animal health certificate is required for the transport of
a) animal products intended for special treatment (treatment), and
use (section 18, paragraph 4, and 5)
(b)) where required under this Act, specific legislation or regulations
The European Union, in the cases of animal products intended for trading
or exports, or in other cases.
(2) Regional animal health management, that issued a health certificate is
shall keep a copy of it for 3 years.
(3) animal products, to whose carriage requires veterinary
the certificate shall be subject to veterinary examination at the place of origin, and
set if the regional Veterinary Administration, also in the place to which the
These products are transported.
(4) Implementing legislation
and in more detail) veterinary requirements for equipment, cleaning and
disinfection of ramps on which loading and unloading livestock products,
on the equipment means of transport which are transported to the animal
products, their cleaning and disinfection and the method of saving the animal
products in their shipping areas
(b)) provides for a time limit within which you can apply for the issue of a health certificate to the
the carriage of animal products, the terms and duration of this
the veterinary certificate, how and on what basis is this veterinary
issuing the certificate.
Section 4
The sale of small quantities of primary products to the final
the consumer
§ 27a
(1) the breeder can in small quantities
a) selling live poultry and live rabbits from the animals on your
directly to the consumer economy for consumption in his household,
(b)) to sell fresh poultry meat and fresh rabbit meat, originating from the
poultry and rabbits on his own holding and slaughtered in this
the economy, in its economy in the market or at the market, and it
directly to the consumer for consumption in his household, or deliver to
local retail stores that supplies this meat as meat
fresh directly the final consumer,
(c)) to sell bulk fresh eggs from your own farm
in its holding in the market or in the marketplace, and it directly
consumer for consumption in his household, or deliver to a local
a retail store that supplies directly to the final consumer;
where the eggs are sold in the market or in the marketplace, or delivered to the
local retail stores, must be marked with the laid down
way ^ 17a); However, this does not apply to eggs from the holding of the keeper,
that behaves most 50 laying hens,
(d)) to sell honey originating from own breeding bees in your home,
in its holding at a bazaar, or hives, the
the marketplace, or to deliver to a retail store that supplies
directly to the final consumer and is in the territory of the County in which is located
the Habitat of the beehives; If the honey sold in the market or in the marketplace,
or delivered to the retail store shall be designated by his name,
last name and address of the keeper, in the case of a natural person, or
the name and address of the keeper, in the case of a legal person, the kind of honey according to the
its origin and indication of its quantity, and if it comes to a retail
retail, also the date of minimum durability
(e)) with the consent of the County to sell Veterinary Administration of the raw, mlékárensky
the untreated milk and raw cream (hereinafter referred to as "raw milk")
originating from animals from animals at the point of manufacture or
through the vending machine, which is located on the territory of the County, in
the breeding of animals, from which the raw milk comes from, or counties
adjacent, directly to the consumer for use in his home. Breeder
shall ensure that raw milk meets the requirements and criteria laid down for the
primary production of raw milk and colostrum European Union regulations governing
specific hygiene rules for food of animal origin ^ 37), and
ensure the examination of raw milk laid down by an implementing regulation
to detect the presence of pathogens affecting health
people, when
1. submission of the regional Veterinary Administration for approval to sell
raw milk,
2. any change in the breeding of animals and any change in the method of obtaining, treating the
and the processing of raw milk, which could affect his health
safety, but at least once a year,
(f)) to sell live fish and other aquaculture animals from the
animals on your farm direct to the consumer for consumption in
his household.
(2) in a local retail store referred to in paragraph 1 (b). (b)), and (c))
considered a retail shop with a corresponding range of animal
products in the village, which is from the municipalities, in which such retail
Shop closest to the holding of the breeder.
(3) animal products referred to in paragraph 1
a) must come from healthy animals and must be wholesome and
safe in terms of protecting human and animal health, in particular, must not be
source of risk spreading diseases and diseases transmissible from animals to man,
(b)) shall not be placed on the market.
(4) the Breeder who sells or supplies its own products from primary production
referred to in paragraph 1, shall ensure that these products were
and manufactured in a clean environment) with the use of equipment and operating
tools and utilities, maintained in the purity,
b) protected from influences that might adversely affect their
wholesomeness, in particular from contamination.
(5) the Breeder who sells raw milk referred to in paragraph 1 (b). (e)), it is
required to handle and comply with the operating and sanitary regulations and on demand
submit it to the regional Veterinary Administration. If it finds the regional veterinary
manage the breeder on the sale of raw milk is inconsistent with the
This law or the regulations of the European Union, the agreement of breeders be withdrawn.
Breeder who sells raw cows ' milk referred to in paragraph 1 (b). (e)),
must further ensure that raw milk meets the sale to the consumer
the criterion for the plate count at 30 ° c in raw cow's
milk for the manufacture of milk-based products, which set out the rules
The European Union governing the specific hygiene rules for food of
of animal origin ^ 38).
(6) the implementing legislation provides for
and veterinary and hygiene rules) for the sale and delivery of small
quantities of primary products, referred to in paragraph 1, and to
treatment with these products,
(b)) what is meant by a small amount of referred to in paragraph 1,
(c) the scope and limits of the investigation) of raw milk for the detection of
pathogenic micro-organisms threatening people's health.
section 27b
(1) the user of hunting ground can the body in small quantities of wild
game in the skin or feathers
and sell directly to the consumer) for consumption in his household, or
(b)) to deliver to a retail store, which supplies directly to the final
consumers and is in the territory of the County in which the beasts are caught, or
(c)) to deliver to retail device that was the regional veterinary
the administration of the registered as device designed for treatment of game meat and
which is on the territory of the County in which the game was caught, or counties
the neighboring.
(2) the body of wild game referred to in paragraph 1 (b). and) or
(b)) shall not be placed into circulation.
(3) the user is obliged to provide a hunting license examination bodies caught free
living game meat referred to in paragraph 1 as soon as possible after being caught, and it
the trained person who is an eligible participant in the hunt. Examination may
also be done by the user, or a member of his hunting license, if they are
trained persons. If caught by wildlife pursuant to
results of the tests carried out by the trained individual health risk,
must be submitted by the official veterinarian to the hunting ground
Veterinary examination.
(4) a hunting license, the user is obliged, upon request of the official veterinarian.
doctor to submit records of wildlife caught sell and own
consumption, according to the law on hunting ^ 7).
(5) the trained person is required to keep records of the types and numbers of
caught and tested for wild game, about the place and time of her being caught,
on the results of the test and about where this game was delivered, store
These records for at least 2 years and provide on request to the official
veterinary surgeon.
(6) in the case of animals susceptible to trichinosis, the user is obliged to a hunting license
to ensure its examination for trichinae (Trichinella), in
the lab, which has been issued a certificate of accreditation for the implementation of this
examination, or at the State Veterinary Institute, or in the lab,
that was the regional veterinary services issued pursuant to § 50 para. 3
permission for this kind of investigation. The laboratory is obliged to issue the
user protocol for laboratory examination of hunting ground game and once
annually submit to the official veterinarian carried out data
examinations provided for in the implementing legislation. The user class is
shall keep Protocol on the laboratory examination of wild game for
at least 2 years of age and present it on request to the official veterinarian
doctors. The user class can animals susceptible to trichinosis sell
or supply to the final consumer in a manner referred to in paragraph 1 to
following a negative examination of wild game on the trichinae (Trichinella).
(7) caught by wildlife, hunting, or authorized by the user
the participant shall apply exclusively for hunting consumption in your household, you may not
the trained person to be examined. In the case of animals susceptible to the
trichinosis, the user is obliged to secure her hunting license examination for
trichinae (Trichinella), in the laboratory referred to in paragraph
6. obligations of the user class and laboratories referred to in paragraph 6 sentence
the second and third shall apply mutatis mutandis.
(8) the trained person is a physical person who graduated from the
specialized training focusing on the investigation of the bodies of hunted freely
wild game, set by the legislation of the European Union), and 17 g ^ gained so
a certificate of eligibility to this activity. The training ensures high
with the veterinary school curriculum, which also trained persons
issues, suspended and withdrawing certificates, keeps a list of such persons and
It passes the Central Veterinary Administration. If it finds the regional veterinary
the Administration in the performance of the State veterinary supervision that the trained person
infringed the obligations provided for in this Act or the regulations of the European
Union ^ f) high school, that the certificate was issued, the incentive to
the suspension or withdrawal of a certificate to that person. Before
the start activity is the trained person to whom the certificate was suspended,
required to submit to a test to validate the expertise of the trained person.
(9) the implementing legislation shall in accordance with the provisions of the European
Union ^ 17 g)
and) the manner and scope of investigation bodies of hunted wild game, the management
records of the trained person and information on examinations, which are
laboratories are required to submit an official veterinarian including
date of their submission,
b) veterinary and hygiene rules for the sale and delivery of small
the quantity of carcasses of hunted wild game, referred to in paragraph 1 and for
treatment with them,
(c)) what is meant by a small amount of referred to in paragraph 1,
d) content, scope and organization of specialized training focusing on
investigation bodies of hunted wild game, method and organization
validation of acquired knowledge, certification and list management
trained people.
TITLE IV
THE ANIMAL HEALTH CONDITIONS FOR TRADE IN ANIMALS AND ANIMAL PRODUCTS WITH
MEMBER STATES, THEIR IMPORT AND TRANSIT FROM THIRD COUNTRIES AND THEIR
EXPORTS TO THESE COUNTRIES
Section 1
Trade in animals and animal products with the Member States
section 28
(1) the subject of trading can only be
and) animals which comply with the requirements provided by this Act,
special legislation ^) and 17q European Union regulations ^ 17r)
in particular, that
1. come from a holding or another registered
under special legislation ^ 8), which is not subject to restrictive or
prohibiting health measures applicable to animals on the
species and is under state veterinary supervision,
2. are healthy and meet the laid down animal health requirements for trade
with them, as well as any special health guarantees ^ m 17s)
3. are identified and registered in accordance with the law plemenářského ^ 9 d) and accompanied by a
a health certificate ^ 17t), and does not require such certification if, other
by the accompanying document,
(b)) animal products which meet the requirements laid down in this
by law, special legislation ^ regulations of the 17u)
Union ^ 14 d), in particular, that
1. come from an undertaking, business, or other device, which is approved and
registered or registered under this Act and the regulations
The European Union ^ 17 h) and is under the State veterinary supervision,
2. are wholesome, at all stages of their production, processing
and putting into circulation of the obligations have been met and the requirements of the
the perspective of the protection of human and animal health and meet the laid down the animal health
requirements for trading with them, as well as any specific animal health
warranty ^ 17v)
3. are marked way ^ 14f) and accompanied by an accompanying
document, or, where required the health certificates, this 17t) ^ ^
certificate.
(2) the subject of trading cannot be animals and animal products,
that of veterinary or health reasons cannot be commercially
used in the Czech Republic, nor animals, which was intended to defeat the
or killed in connection with the implementation of the programme of recovery of animals or
in the context of conservation and control measures.
(3) animals and animal products referred to in paragraph 1 shall be subject to
veterinary inspection at the place of origin and veterinary inspection upon arrival
to the place where they are accompanied by a health certificate, as appropriate,
other accompanying document, and in which they are received (hereinafter referred to as "instead of
determine "). Their veterinary check at the place of origin shall be carried out
at least with such care and responsibility, as if they were
intended for the domestic market. The health inspection upon arrival to the place of
the determination is carried out by means of non-discriminatory random checks ^ 17w).
(4) persons who are involved in the trade of animals and animal
products are required to ask the regional health administration of the
registration. However, this does not apply to persons who have already been receiving regional subsidies
Veterinary Administration approved and registered under section 9b or under section 22
paragraph. 1 (b). and regional animal health management) registration cancelled if
registered person seriously or repeatedly violates the obligations of the
provided for in this Act or the regulations of the European Union.
(5) the implementing legislation shall specify a period within which you can apply for
the animal health certificate which accompanies the animals and animal products
referred to in paragraph 1, the terms and period of validity of this certificate and
how and on what basis is this certificate is issued.
section 29
Veterinary checks at origin
(1) the health inspection at the place of origin to determine whether
and) sent the animals and animal products meet the set sent
the conditions for trading, and if these conditions have not been established, the conditions of
required by the State of destination, and that sent the animals are transported in
appropriate means of transport meeting the requirements on hygiene
their transport and to their well-being,
(b) the keepers of such animals comply with) the requirements laid down in their breeding
and whether the persons handling these animal products shall comply with the
the requirements for producing them and dealing with them.
(2) the breeders and people who handle animal products, are
obliged to provide authorities carrying out veterinary inspection in place
the origin of the necessary cooperation and assistance in particular in the implementation of the health
tests, sampling and inspection of documents.
section 30
Veterinary checks on arrival at destination
(1) the health inspection upon arrival at the place of destination, in particular, verifies the
and performing spot checks whether) the incoming animals and coming
animal products meet the specified conditions for trading, and
If these conditions have not been established, the conditions required by the Czech
Republic; random control samples may be taken
(b)) the control of the animal health certificate, as appropriate, other accompanying
the document, whether they are in Assembly centres and markets taken
and in the slaughterhouse are slaughtered only animals which fulfil the conditions laid down in
(a)),
(c)) that are accepted in businesses, factories or other facilities under
the State veterinary supervision only animal products whose description
and the required accompanying documents comply with the requirements referred to in
(a)),
(d)) if it should happen that the animals after arrival at destination
of the disease reasons placed and kept in quarantine.
(2) if the authorities in charge of veterinary inspection upon arrival at the
place of destination
and the presence of agents of the diseases referred to) in section 10, paragraph 1. 2 the first sentence, the disease
transmitted from animals to humans or other disease or other
the cause of a serious threat to animal or public health, or that the
animal products originate from areas infested with rapidly spreading
disease, shall decide on the location of the animals in quarantine or slaughter
or killing, or of the disposal of animal products,
(b) failure to comply with the conditions laid down for the) trading, may retain,
If permitted animal and public health conditions to the sender,
to choose one of the following measures: the location of the animals and
animal products under veterinary supervision to eliminate
their non-compliance with the conditions laid down, the slaughter or culling
animals or destruction of animal products, the return of animals
or animal products, with the agreement of the competent authority of the State of origin,
where appropriate, the prior consent of the transit State, or use the
animal products for other purposes. If the sender does not use options
the choice of one of these measures within a time limit specified by the authorities
veterinary checks on arrival at destination, shall decide on the appropriate
measures of these institutions. However, if the reason for this procedure errors
or irregularities in the veterinary certificate, or in another
the accompanying document, the sender of the first must be granted a period of
the removal of these deficiencies.
(3) the recipient animals and animal products at destination are required to
and advance the regional animal health) to inform the Administration about the arrival of the animal or
animal products from another Member State, to the extent necessary
of the purpose and the method of carrying out the veterinary checks on arrival
at the place of destination,
(b)) control before splitting, or commercial exploitation of the consignment, whether
are animals or animal products laid down by the manner and
accompanied by the required supporting documents, and any misconduct or
notify without delay the regional discrepancies of the Veterinary Administration,
c) keep records of the underlying stores, keep these records,
the animal health certificate and other accompanying documents for at least 1 year and
on request, submit to the official veterinarian,
(d)) to provide veterinary control authorities upon arrival at the
instead of specifying the necessary cooperation and assistance, in particular when examining
documents.
section 31
(1) If on the territory of the Czech Republic to the occurrence of diseases listed in § 10
paragraph. 2 the first sentence, the disease transmissible from animals to humans or other
of illness, or to another possible cause of a serious threat to animal health
or the people, it shall inform the Commission and the State Veterinary Administration Member
States.
(2) costs related to the measures referred to in section 30 paragraph 2. 2 bears without the right to
compensation from the State to the consignor or his representative.
(3) Implementing law provides
and animal health requirements for) a specific trade in animals
each of the species and a variety of animal products,
(b)) a way of implementing the veterinary checks at origin and veterinary
checks on arrival at destination, the cooperation and assistance which are
obliged to breeders and people handling animal products
provide authorities carrying out such checks,
c) details of the measures, which shall be the veterinary authorities
control based on the finding that the conditions laid down are met for
trading, as well as the procedure in the case in connection with these
measures to the dispute between the sender and the authorities
veterinary checks on arrival at destination,
d) range and other essentials of the data disclosed that authorities
carrying out veterinary inspection shall immediately be communicated through
remote data transfer,
e) details of the procedure and the synergy with the State Veterinary Administration
the competent authorities of the Member State of origin, in the cases referred to in section 30
paragraph. 2.
§ 31a
(1) the provisions of sections 28 to 31, with the exception of movements under section 4A(1). 2
not apply to non-commercial movements of pet animals as referred to in
part A of annex I to the regulation of the European Union concerning animal health conditions for
non-commercial movements of pet animals ^ 48). The movement of these
animals from other Member States to the United Kingdom is governed by the law
The European Union on the animal health requirements applicable to non-commercial movements of animals
Pet ^ 48).
(2) pet animals referred to in paragraph 1, which are under
twelve weeks and not vaccinated against rabies or are aged between
twelve and sixteen weeks, are vaccinated against rabies, but has not yet
do not meet the requirements for the entry into force referred to in paragraph 2 (a). e) Annex III
Regulation of the European Union concerning animal health conditions for non-commercial
movements of pet animals ^ 48) can be moved within the
the non-commercial movement from other Member States, are met.
conditions laid down in article 4(1). 7 of the European Union on veterinary
conditions for non-commercial movements of pet animals ^ 48).
(3) the Central Veterinary Administration may, at the request of the keeper in accordance with
article. 32 para. 1 of the European Union concerning animal health conditions for
non-commercial movements of pet animals ^ 48) allow repositioning
the pet animal referred to in paragraph 1, which does not meet the
the conditions laid down in paragraph 1 and fix the conditions of such transfer.
(4) the Control of pet animals referred to in paragraph 1 in accordance with article 3(1).
33 European Union legislation concerning animal health conditions for non-commercial
movements of pet animals ^ 48) take the form of non-discriminatory
a spot check by the regional Veterinary Administration. If animal control
found a violation of the requirement laid down by the EU regulation
animal health requirements applicable to non-commercial movement of pet animals
breeding ^ 48), regional Veterinary Administration decides, pursuant to article. 35 regulation
The European Union on the animal health requirements applicable to non-commercial movements of animals
Pet ^ 48).
Section 2
The importation and the transit of animals, animal products and other health
goods from third countries and their export to these countries
Imports from third countries
§ 32
(1) animals, animal products and other animal goods imported from
third countries (hereinafter referred to as "controlled goods") may enter the territory
The United States only through veterinary border control station of the Czech
Republic of China (hereinafter referred to as "border veterinary station") or another
of a Member State. Animals shall be transported directly to this post
or the quarantine centre and from there to the destination indicated in the
the animal health certificate, as appropriate, in another document, which
the consignment is accompanied by them.
(2) the controlled goods referred to in paragraph 1 shall be considered as also mixed
products, which means food intended for human consumption containing
as processed products of animal origin and products of vegetable
of origin, including those for which the processing of the primary product is an integral
part of the production of the final product.
(3) border veterinary station, that is either directly at the point of entry
on the territory of the Czech Republic or in its vicinity, is part of the regional
Veterinary Administration, to which it is locally relevant. Its operation is governed by
a production order issued in agreement with the Customs authorities and the authorities of the police
Of the Czech Republic.
(4) each consignment checked goods must be accompanied by the original of the
the veterinary certificates or other veterinary documents or other
documents required by this Act or the regulations of the European Union;
the originals of these documents shall be kept at the border inspection
the station. Controlled goods are on border veterinary station
subject to border veterinary inspection to ensure that they are
fulfilled animal and public health requirements for imported
controlled goods (hereinafter referred to as "terms"). It shall be carried out by an official
County veterinarians Veterinary Administration, a part of which is
boarder veterinary station (hereinafter referred to as "the authorities in charge of border
veterinary inspection "), who are responsible for the implementation of the border
veterinary checks; in its implementation, as well as after its implementation,
follow this law, special legislation ^ 17) and
European Union legislation 17y ^ ^).
(5) the authorities in charge of border veterinary inspection shall be issued after
the implementation of this control to the person who submitted the item to checked
check the copy of the common veterinary entry document
(CVED) ^ z) (hereinafter referred to as "entry document").
(6) the Customs authorities shall release the controlled goods for free
circulation ^ 18), where the Declaration was not substantiated by the input document, which
confirms that a border veterinary inspection has been carried out with the
a favourable outcome and that are paid for the costs associated with border
veterinary check, or that was paid and the deposit
costs connected with the measures referred to in § 34 paragraph 1. 2 and § 35 para. 1.
(7) the importer or his agent, or other person responsible for the
the cargo shall prior to arrival of the shipment in the territory of the Czech Republic
and inform the border inspection station) through the input
document
1.1 business day in advance of the arrival of the imported animals to this
the station, with an indication of their number and the type and the expected time
their arrival,
2. in advance of the arrival of imported animal products and other
Veterinary goods on this station, and this, together with their weight and
the type and the expected time of their arrival,
(b) submit to the controlled goods) with the necessary accompanying documents, and
information for the implementation of the border veterinary checks on the spot, on the
which has to be checked, and give the authorities
This check at their request, the necessary cooperation and assistance
(c)) where they are the subject of the importation of animals or animal products for which
the import conditions have been established (harmonised) at the level of
The European Union, requested in advance the central veterinary administration of the communication
the import conditions, which are applicable to imports of animals or
animal products of the species from the third country concerned or its
part of the United Kingdom and comply with any
terms and conditions.
(8) the authorities of carrying out border veterinary control are not liable for
the damage, which occurred an indispensable means of transport delays in
as a result of performing this check. In its implementation, however, progress
so that was the operation of the carrier or the postal service
disturbed more than is strictly necessary.
(9) specific legal provisions on the importation of animals ^ 18a) and on the conditions of their
transportation ^ 6) shall remain unaffected.
the title launched
§ 33
(1) border veterinary control includes checking documents and
the identity of the controlled goods and physical control.
(2) the control of documents and the identity of the controlled goods shall be verified
and, the origin and subsequent destination) of the imported animals and whether the information given
in the veterinary certificates and other accompanying documents confirmed
import requirements and whether the consignment was not rejected,
(b)) whether imported animal products and other animal health goods
correspond to the data indicated in the veterinary certificate and in the other
the accompanying documents.
(3) physical control of imported
and includes their clinical) animals and the necessary laboratory examinations,
as well as the verification of compliance with the requirements for their protection during
transportation ^ 6). If necessary, it also performs the subscription
the samples to be investigated, and in particular for the presence of residues,
(b)) of animal products and other veterinary goods includes their
sensory examinations, sampling and laboratory testing, which
to determine whether these products and other goods correspond to the import
conditions and whether they are in such a condition that they can be used for a purpose
as is indicated in the health certificate, as appropriate, in the other accompanying
documents.
(4) If a suspect that the import conditions are not complied with, or
If in doubt about the identity or status of controlled goods
authorities shall carry out border veterinary control of any
further investigations that they deem necessary in the interests of the responsible fulfilment of
the purpose of this check.
(5) if the authorities in charge of border veterinary control, that
and) controlled goods is dangerous for public or animal health,
1. shall provide adequate suitable measures to prevent further exposure, and
the spread of risk to public or animal health,
2. inform the findings and the measures taken and the origin of
the item other frontier veterinary station and the Commission,
(b) the activities of a unit) in the veterinary border control
another Member State are manifested serious or repeated shortcomings,
shall take the appropriate measures to inform the Commission and the Member States of the
These deficiencies.
(6) the implementing legislation provides for
and the location of the border veterinary station) and the details of
their basic material and personnel security,
(b) the place and method of performance) of the border veterinary checks, including
establishment of the procedure in the case of veterinary checks of goods for
Import via another border inspection post, or intended for
another Member State, and measures which make the authorities in charge of border
a veterinary inspection on the basis of the results of this check,
c) details of the measures, which makes the border authorities
veterinary inspection based on a finding that the import are not met
conditions,
d) range and other essentials of the data disclosed that authorities
carrying out veterinary inspection shall immediately be communicated through
remote data transfer,
(e)), which provides a range of synergies, the importer or his representative
border veterinary inspection authorities.
Importation of animals
§ 34
(1) the entry of animals imported from third countries on the territory of the Czech Republic
cannot be enabled if the
and) the animals for which import conditions have been established (harmonised) on
the level of the European Union, come from a third country or part thereof that
is not listed on the list of third countries and parts thereof, from which they can be
animals of the species imported, or from a third country or part thereof from which
the importation of animals of the species is prohibited,
b) animals for which import conditions have been established
(harmonized) at the level of the European Union, do not satisfy the import conditions
applied in the Czech Republic,
(c)) the animals are sick disease or diseases transmissible from animals to
a man suspected of being infected or of diseases transmissible from animals to man,
or are from another because of danger to human health or the
animals,
d) animals are not in good enough condition that would allow them
continue their journey,
e) veterinary certificates or other accompanying document does not meet the requirements of the
set for the document, which shall accompany the animals imported from third countries,
(f)) the exporting third country does not meet the requirements established for third countries
exporting animals in the Member States.
(2) if required by this Act or the regulations of the European Union,
the imported animals placed in quarantine or isolation, the quarantine
or isolation may take place in an approved quarantine centre third country
of origin, at a quarantine centre in the Member State or at the farm
destination. They are to be imported animals placed in quarantine on the basis of
the result of the border veterinary checks shall be determined by the authorities in charge
border veterinary inspection with a view to their perceived
the risk of whether the quarantine will take place on the border veterinary
station or in its immediate vicinity, or in the economy
destination or at a quarantine centre situated in the vicinity of the
the holding of destination. '.
(3) the costs of the location and the keeping of animals in quarantine or isolation, which
taking place in the border inspection post shall be borne without
compensation from the State, the importer or his representative, the cost of the location and
the keeping of animals in quarantine or isolation in other cases bear no
compensation by the State of the recipient.
(4) trade in animals that have been imported from a third country, the
frontier veterinary station and was released for free circulation,
governed by the rules set out in title IV, section 1; If circumstances so require,
It is carried out the health inspection of animals at the time of arrival
destination.
(5) Implementing law provides
and the specific requirements for importation) animals of various species from third countries and
details about the reasons that prevent the entry of each species of animals
imported from third countries on the territory of the Czech Republic,
(b) the placement of the animals) imported from third countries in quarantine or isolation
and veterinary and technical conditions for the approval of quarantine
of the Centre.
the title launched
§ 35
(1) if border veterinary checks show that the animal
imported from a third country do not satisfy the import conditions, or that there has been
other misconduct or irregularity, the authorities in charge of border
veterinary supervision, after consultation with the importer or his representative
a) determines that the animals will be
1. temporarily housed, fed, watered and, where necessary, treated,
or
2. placed in quarantine or isolation, and
b) decide that the animals will be
1. sent back within the prescribed period, unless their
health status or requirements for their well-being, while at the same time cancels the
the validity of the health certificate or any other accompanying document,
accompanying the rejected consignment, or
2. Veterinary examination, and in accordance with the results of the Veterinary examination
slaughtered for the nutritional needs of the people, or be killed.
(2) the importer or his representative shall be liable without compensation from the State
costs connected with the measures referred to in paragraph 1, after deduction of the
any revenue from the sale of slaughter of the animal obtained animal
products.
Import of animal products
section 36
(1) animal products imported from third countries, must satisfy the requirements
referred to in § 18 para. 1 and 2 and in the regulations of the European Union ^ 18b), or
providing equivalent guarantees. Animal health certificate which accompanies them,
must certify that the animal products satisfy the import conditions, including
any special import conditions if such conditions were
institutions of the European Union established for the relevant third country or group
third countries.
(2) products of animal origin imported from third countries, which have entered the
the territory of the Czech Republic, without having been presented to the border inspection
checks must be confiscated and either disposed of or returned.
(3) if the border veterinary checks show that the animal
products imported from a third country do not satisfy the import conditions, where appropriate, that
Another misconduct or irregularities, the enforcement
border veterinary inspection after consultation with the importer or his
representative decide that these products will be
and sent no later than) 60 days back, unless the result of the
border veterinary checks or animal and public health
requirements, through the same border inspection station, and if
possible, using the same means of transport. In this case, the authorities of the
performing the border veterinary inspection also invalidates the
animal health certificate or any other accompanying document, which
accompanying the rejected consignment, or animal products cannot be send
back, passed the period of 60 days or credit to the importer or his
the representative of the instant approval
b) disposed of.
(4) until a postback or disposal must be
animal products under state veterinary supervision.
(5) pursuant to paragraph 3 shall take place, if it has been enabled using the
animal products for any other purpose, provided that this does not jeopardise the health
people or animals.
(6) the importer or his representative shall be liable without compensation from the State
costs connected with the measures referred to in paragraphs 2 to 4.
§ 37
the title launched
(1) animal products imported from a third country and intended for free
zone, the free warehouse ^ 19) or a customs warehouse ^ 20)
the perspective of the border veterinary checks are considered goods intended for
release for free circulation in the territory of the United States or other
Member State, unless they are clearly intended to another final
the use of the. Therefore, they are subject to border veterinary border station
veterinary inspection for the purpose of checking compliance with the import conditions.
(2) the re-entry of animal products, which have been rejected by a third country,
You can enable, if these products
and shall be accompanied by the original) of the health certificate, as appropriate, its
copies certified by the authority which issued the certificate, together with an indication
because of the rejection of the shipment and the guarantee that these products was not
treated and that comply with the animal health conditions laid down for their
storage and transport, and in the case of sealed containers
the carrier's statement that those products has not been treated and that the
the contents of the containers unloaded,
(b)) are subjected to documentary and identity checks, and if
doubts as to their compliance with the import conditions, whether or not
physical check
(c)) have been returned from the border veterinary station directly undertaking, business,
where appropriate, to another establishment of origin, in sealed vehicles with
water-proof parts, intended for the carriage of livestock products, or in the
sealed, leak-proof containers. In the case of transit through the territory of
another Member State, the authorisation of reimportation, be conditional on the
such transit has been previously authorised on behalf of all the Member States whose
the territory of the shipment, the official veterinarian of the Habitat
veterinary border inspection post in the Member State in which the products for the first time
entered the territory of the Member States.
(3) persons that supply animal products intended for consumption
the crew and passengers on the vessel in the international maritime
transport, must
and for this purpose) be approved by the regional veterinary services and
registered,
(b)) have available space for storing animal products
controlled entrances and exits,
(c)) guarantee that does not release the animal products that do not meet the established
conditions for consumption in the territory of the Czech Republic or another Member
State.
(4) trade in animal products, which were imported from a third
the country has undergone a frontier veterinary station and put into
free circulation, shall be governed by the rules laid down in title IV, section 1;
If circumstances so require, the health control of these
products on arrival at destination.
(5) Implementing law provides
and the specific requirements for importation) of different animal products from third
countries, including the requirements applicable to imports of products destined for free
zone, a free warehouse or a customs warehouse, and on their border
veterinary inspection,
(b)) the details of the return of animal products that have been
rejected by a third country, and direct provision of animal products intended
for consumption by the crew and passengers on board the vessel in the international maritime
transport.
§ 38
The transit of animals and animal products from third countries
(1) the transit of controlled goods from one third country to another third
country (hereinafter referred to as "transit"), the territory of the Czech Republic shall apply the provisions of § 32,
33, 35 and 36.
(2) the transit of animals may be authorised, provided that the
and) those animals originate from countries in which animals not allowed
on the territory of the United States, and that they meet according to the results of the border
veterinary checks on import conditions, or terms at least
equivalent, or that transit these animals was no longer authorised by the official
veterinarian veterinary border inspection post of another
the Member State on whose territory the animals were submitted to the border
veterinary inspection before
(b)) is in accordance with local legislation, proof of commitment
the first of the third countries where animals are being sent, after transit through the territory of
The United States, that these animals will not refuse under any circumstances and
to send back, as well as compliance with the requirements for their protection
during transport,
(c)) the animals are transported in the manner and under the conditions, which correspond to the
the veterinary requirements for their transport, and that in the course of carriage
are carried out with regard to the treatment of these animals, only activities
which are carried out at the point of entry or exit from the territory of the Czech Republic,
and activities necessary to ensure the welfare of animals,
(d)) for information about how these animals have passed through border inspection
the station is via remote data transmission transmitted to the competent
transit authorities of the States concerned and the veterinary border inspection post
the checks, which the animals leaving the territory of the Member States.
(3) transit of animal products may be authorised, provided that the
and) those products originate in a third country in which the product was not banned
entry into the territory of the Czech Republic, and that they meet according to the results of the border
veterinary checks on import conditions, or that the transit of these products
has already been authorised by the official veterinarian of animal health unit
border inspection post of another Member State on whose territory these
products submitted to the border veterinary inspection before
(b) the person responsible for the consignment) these products undertake it again
takes over, if it will be rejected, and that these products be disposed in accordance
with § 36 and pay fees for the implementation of the border veterinary checks.
(4) Implementing legislation laying down animal health and public health requirements
on the authorisation of the transit of various types of controlled goods and the method of
the implementation of the border veterinary inspection of the item.
§ 38a
(1) the provisions of § 32 to 38 shall not apply to products of animal origin referred to in
Regulation of the European Union on the importation of consignments of products of animal origin for
personal consumption into the community ^ 21). The import of consignments of such products,
governed by the law of the European Union on the import of a consignment of products of animal
origin for personal consumption within Community ^ 21).
(2) the inspection of animal products referred to in paragraph 1 in accordance with article 3(1). 5 and
6 the European Union regulation on the importation of consignments of products of animal origin
for personal consumption into the community) are carried out in 21 ^ ^ under tariff
control of the Customs authorities, in checking passengers and their personal
baggage and for the control of imported shipments for postal operators
services and operators of courier services. Where the Customs Office when the
check at the point of entry, the shipment of animal products does not meet the
conditions laid down in the EU regulation on the import of consignments of products
of animal origin for personal consumption within Community ^ 21), have fun
shipment and proof on its seizure.
(3) the Customs Office checks whether the operators of all points of entry to the territory of
The United States comply with the obligations referred to in article 14(2). 3 and 4 of the
The European Union on the import of a consignment of products of animal origin for personal
to the Community consumption ^ 21).
(4) the provisions of § 32 to 38 shall not apply to the animals referred to in annex I
Regulation of the European Union concerning animal health conditions for non-commercial
movements of pet animals ^ 48). Imports of these animals shall be governed
the EU regulation on the animal health requirements applicable to non-commercial
movements of pet animals ^ 48).
(5) control of the animals referred to in paragraph 4 in accordance with the provisions of article. 34
Regulation of the European Union concerning animal health conditions for non-commercial
movements of pet animals ^ 48) at the point of entry into the territory of the United
States shall be carried out within the framework of the customs control the Customs authorities, in checking
passengers and their personal baggage. If animal control
found a violation of the requirement laid down by the EU regulation
animal health requirements applicable to non-commercial movement of pet animals
breeding ^ 48), shall inform the Office of the provincial health administration. Regional
animal health management decides on the consignment referred to in article. 35 regulation
Union concerning animal health conditions for non-commercial movements of animals in
Pet ^ 48).
(6) the Customs authorities during the checks referred to in paragraph 5 shall keep records of
the total number of inspections carried out and on cases of non-compliance with the conditions
These inspections identified under article 3(2). 34 para. 4 (b). (b)), and
shall record the information referred to in article. 34 para. 4 (b). (c)) of regulation
Union concerning animal health conditions for non-commercial movements of animals in
Pet ^ 48).
(7) pet animals listed in part A of annex I to Regulation
The European Union on the animal health requirements applicable to non-commercial movements of animals
Pet ^ 48) that are under the age of twelve weeks and are not
have been vaccinated against rabies or are between the ages of twelve and sixteen
weeks ago, are vaccinated against rabies, but still do not meet the requirements for
force referred to in paragraph 2 (a). e) of annex III to regulation of the European Union on the
animal health requirements applicable to non-commercial movement of pet animals
breeding ^ 48), may be imported under the non-commercial movement from third countries
in the United States, are subject to the conditions laid down in article 4(1). 11
Regulation of the European Union concerning animal health conditions for non-commercial
movements of pet animals ^ 48).
(8) the Central Veterinary Administration may, at the request of the keeper in accordance with
article. 32 para. 1 of the European Union concerning animal health conditions for
non-commercial movements of pet animals ^ 48) allow the importation of an animal in
pet animals listed in part A of annex I to the regulation of the European Union on the
animal health requirements applicable to non-commercial movement of pet animals
breeding ^ 48) that does not meet the conditions laid down in article 4(1). 10 Regulation
The European Union on the animal health requirements applicable to non-commercial movements of animals
Pet ^ 48) and to determine the conditions of such imports.
section 38b
The export of animals and animal products to third countries
(1) the export of controlled goods to third countries will be required
the animal health certificate. To the exporter's request for his extradition must be
proof of health conditions, compliance with which requires
importing or transit State, in an authenticated translation.
(2) if the third country refuses a consignment and if it returns,
shall be borne by the exporter without compensation by the State, the costs associated with this
measures.
(3) if the third country of destination requires a health certificate, printed on
ceninovém paper with protective characters, will pay the costs of the exporter
its printing. On the compensation for the costs associated with printing, veterinary
certificate for export of regional Veterinary Administration decides. This compensation is
State budget revenue, it selects the regional animal health management, which
It has imposed. The amount of the flat-rate amounts for the costs associated with printing
veterinary certificate for export shall adopt detailed legislation.
(4) if the third country of destination requires verification of health certificate to the
the exports of the central competent authority, makes it the central veterinary
Administration.
(5) the implementing legislation provides for a procedure in case of refusal, and
return of the shipment to a third country, as well as the time-limit within which to apply for
veterinary certificate for export, the period of validity of the certificate, as
and on what basis is this certificate is issued.
section 38 c
(1) for the carriage of goods at controlled imports, exports and transit may
only be used if such means of transport, equipment, and packaging that
satisfy the animal health requirements laid down for national transport
goods of the same kind.
(2) power supply and feeding the animals at the border inspection post,
where appropriate, in other places during transport must be done
to transported animals have not been in direct or indirect contact with
domestic animals.
(3) the transport of controlled goods in the territory of what will
quickly as possible and, if possible, without reloading. Imported animals for slaughter must
be transported directly to the slaughterhouse and slaughtered without delay.
(4) if the duration of the transport of the animals to be exported may not exceed 8 hours, shall draw up
the carrier by the shipper in the agreement with the travel plan.
(5) the implementing legislation to what time after arrival at the slaughterhouse
must be slaughtered imported animals for slaughter by species.
§ 38d
Unless otherwise stated, is not subject to border veterinary control
the item that is under a special legal regulation ^ 23) are exempt from
the checks carried out by the Customs authorities.
TITLE V OF THE
VETERINARY SANITATION
§ 39
(1) the animal health asanačními activities are
and) the collection (collection), transport (cartage), disposal and other
the processing of animal by-products,
b) disinfection, disinfestation, fumigation, or deodorisation,
c) capture of stray and abandoned animals ^ 23a) and their introduction into
quarantine or isolation.
(2) rendering the activities referred to in paragraph 1 can be exercised
only with the permission of the State Veterinary Administration.
(3) animal by-products which are not suitable for animal feed
or further processing, it must be disposed of without delay
by burial at a specified location or by incineration, or harmlessly
removed by another, this Act and the regulations of the European Union ^ 9b) fixed
way.
(4) for disinfection, disinsectization and dezodorizaci, according to this
the law can be used only registered medicines and procedures or
products put into circulation has been enabled ^ 5).
(5) the implementing legislation provides for taking into account the nature of the disease and
the danger of its spread, that preparations and procedures apply when
the implementation of conservation and control measures.
§ 39a
(1) principles of the classification of animal by-products, animal health and
health rules for the collection (the collection), transport (cartage),
labelling, storage, disposal, use and other
the processing of animal by-products of each category,
as well as for the marketing of these products and products made from them into circulation for the
trading with them and for their import, transit and export, provides
European Union regulations ^ 9b).
(2) if the legislation of the European Union ^ 9b) require that secondary
animal products disposed of or further processing, it must be
so state, if not otherwise specified, in the enterprise, establishment or another
the device, which was for disposal and other handling
of animal by-products of its category approved by the State
veterinary services and registered under the veterinary assigned
the approval number. The conditions of approval and suspension, or
withdrawal of approval, are laid down in European Union regulations ^ 9b).
(3) operators of approved undertakings, businesses, or other
the device referred to in paragraph 2, shall, in the harmless disposal
and further processing of animal by-products and a custom
checking the hygiene conditions of this activity under this Act, and
European Union legislation ^ 9b).
(4) the official veterinarian at the approved enterprises, plants,
where applicable, other devices, referred to in paragraph 2, shall, in the
the performance of the State veterinary supervision pursuant to this Act and regulations
The European Union ^ 9b).
section 40
(1) the Keepers and persons handling animal products are required to
to ensure the disposal of animal by-products which
arise in the course of their work or in their establishment; It
shall apply mutatis mutandis also to the operators of airports, ports and other locations
entry into the United States, in the case of imported animal products,
where appropriate, other veterinary goods seized in accordance with the provisions
The European Union ^ 21) and intended to be disposed of, or on the kitchen
waste from means of transport in the international transport. If it is not
unless otherwise specified, are required to
and immediately report occurrence) of animal by-products to the person
who carries out their collection (collection) and transport (cartage). Reporting
the obligation is not a breeder or person handling animal products,
If the person to whom it was granted performance rendering activities,
the Council has agreed on a regular (turnusovém) collection of animal by-products
products,
(b)) sort, label, securely store, and if necessary take care
animal by-products into the transit times for disposal on the
places with which the agreed regional animal health management,
so, in order to avoid their alienation, to the threat to human and animal health
or damage to the environment,
(c)) to keep trade and other papers, relating
animal products are passed to the carriage, for at least 2 years, and
in the case of carcases of animals individually referred to in accordance with special
^ Law 9 d), ensure that the carcasses have been passed down to the
transport including the identification of resources,
(d) animal by-products) to pass to the person who performs their
the collection (collection) and transport (cartage), to provide it with the necessary
cooperation and assistance, particularly as you zoom in on places of carcasses
accessible means of transport and their management, and pay her for
transport and disposal and other handling of miscellaneous
animal products an agreed price.
(2) the Keepers and persons handling animal products, for which
commonly found animal by-products are obliged to
and establish a watertight, well) to clean, disinfect and
sealable with carcass disposal boxes for short-term storage Misc.
animal products, to clean and disinfect them after each flush,
(b) appropriately place the carcass recycling boxes) both in terms of their separation from the
the other premises, as well as in terms of loading and transport
of animal by-products.
(3) unless I know the breeder, has the obligation under paragraph 1
(a). and the one to whom it belongs) or who manages the place of finding of the carcase. In
this case bears the costs of disposal of the carcase.
(4) failing the State Veterinary Administration of the disease reasons otherwise,
can the breeder himself disposed of on land owned by the carcase
the pet animal, if this does not come from the animal's carcase
payable between the ruminants or pigs, or from an animal sick
a dangerous infection or suspected of the disease. Harmless
deleting in this case means the burial spot of the appropriate
the perspective of the protection of human and animal health and the protection of the environment, and
it to a depth of at least 80 cm with the use of disinfectants.
The carcase of a horse breeder, pet can harmlessly delete itself on
private land only with the consent of the regional veterinary service and
conditions laid down by; the breeder is also required to place of burial
of the carcase of a horse in the manner prescribed mark implementing regulation
and this designation to maintain for a period of 10 years.
(5) an entrepreneur, who treats animal products, you may
the approval of the regional Veterinary Administration and under the conditions laid down by the legislation of the
The European Union ^ 9b) to handle in your own device side animal
products that have arisen in connection with its activities.
§ 41
(1) the person to whom the performance of rendering has been enabled, the
required to perform it, so that there is no threat to human health and the
animals, cruelty to animals, or damage to the environment. Person,
the subject of activity is the collection, transport, harmless
disposal and other handling of animal by-products (
"rendering the undertaking"), is required to further
and to ensure continuous reception) to reports of animal by-products
products and collecting them in the 24 hours after he was of their presence
informed, without delay, in cases of public interest,
(b) collecting and harmlessly delete) or further process any side
animal products from the specified jurisdiction (svozové area)
If these products were not in accordance with this Act and the regulations
The European Union ^ 9b) disposed of or otherwise further processed, and
request for payment of the price agreed according to a special legal
prescription ^ 24),
(c)) to do when fighting dangerous diseases or diseases transmitted from
animals to humans and their consequences in accordance with mandated protective and
zdolávacími measures
(d) draw up a code of conduct) and submit it prior to the activity
the regional Veterinary Administration for approval,
e) comply with the animal health requirements for harmless
delete, and other processing of animal by-products of
laid down by this law and the regulations of the European Union ^ 9b), as well as procedures
based on the hazard analysis and critical control points (HACCP),
f) carry out their own checks on compliance with veterinary and health
requirements for disposal and other handling of miscellaneous
animal products laid down in this law and the regulations of the European
Union ^ 9b), keep records of the results of those checks, keep them after
for at least 2 years and present them at the request of the official veterinarian
doctors,
g) create conditions, including free provision of suitable space to
implementation of the pathological-anatomical dissections of carcases (hereinafter referred to as
"the animal health prosektorská activities") of the provincial veterinary services,
h) in the case of carcases of animals individually marked in accordance with the Special
^ Law 9 d), nesnímat, or not to dispose of the identification
resources before for their own disposal or
further processing of the carcasses.
2) animal by-products taken to rendering the undertaking destruction
delete or further processing must not leave the premises of this already
company without the consent of the regional Veterinary Administration, unless their
transfer to another rendering of the business.
(3) a place designated for the disposal of animal by-products
pet products (hereinafter referred to as "zahraboviště"), a device designed for
disposal and other handling of animal by-products
products or place designated for storage or incineration of animal carcases
of pet animals shall be established after consultation of the regional office, the municipal
Office or the regional office and the újezdního of the veterinary service on the spot,
and) enough away from places where they are kept
farm animals,
(b) where this activity will not be) respected the environment.
(4) a device designed for harmless disposal and other handling
of animal by-products shall be equipped and maintained to
allow safe working and safe disposal and processing
the following products, where appropriate, the circulation of such products, which
do not contain unacceptable amounts of harmful substances or of pathogenic
micro-organisms. This device must not be manufactured products intended for
human consumption.
(5) the implementing legislation may provide that, where required under legal acts
The European Union,
and animal and public health) more detailed labelling requirements
the collection (collection), transport (cartage), disposal and other
the processing of animal by-products, to the layout and equipment of
undertaking, business, or other device designed for harmless
disposal and other handling of animal by-products,
zahraboviště and on the device (s) specified for the storage or incineration
carcasses of pet animals, if these requirements are not established
regulations of the European Union,
(b)) the details concerning the implementation of health own checks
conditions of disposing and processing side
animal products operators of undertakings, businesses, or other
the device referred to in § 39a para. 2.
§ 42
(1) the person was allowed to exercise the activities referred to in § 39 para. 1 (b).
(c)),
and in the context of trade and) disease control measures capture of stray and
stray dogs and cats, or other, to the danger of contagion
susceptible animals in the place and time regulation the prohibition of the free movement of animals,
(b)), at the request of the village, in the case of the city of Prague at the request of the city
parts of the capital city of Prague, the Czech Republic Police or municipal police
and in synergy with them the capture of stray and abandoned dogs and cats,
where appropriate, other animals, and placing them in quarantine or isolation,
If their capture in order to protect human and animal health, where appropriate, in
other public interest.
(2) the capture of stray and abandoned dogs and cats, or even other
the animals referred to in paragraph 1, as well as the collection and disposal of carcasses
pet animals, can carry out an individual who graduated from the
specialized professional training, with a focus on this activity
organized College with the veterinary curriculum,
She passed the final examination and certificate of competence to
This activity. Take care of stray and abandoned animals in shelters for
animals can only people who have that certificate.
(3) the person referred to in paragraph 1 or 2 of the trapped animal
and the owner, who shall issue) is obliged to keep this animal according to the instructions
the regional Veterinary Administration after the necessary period in quarantine
(b)) spent, if it decides so regional animal health management of the disease or
diagnostic reasons, if required by the nature of the danger of the disease and
circumstances of the case; the cost of culling ^ 6) of the animal shall be borne by the State.
(4) the costs of the capture of the animal and the temporary care of the breeder
odchyceného of an animal shall be obliged to replace the person that these costs
expended.
(5) if I know the breeder, which trapped the animal should be returned
in accordance with paragraph 3 (b). and), or if you cannot return it to the producer from another
because, the person referred to in paragraph 1 or 2 of the trapped animal
and the Civic Association) will offer, which participates in the execution of the tasks of the protection
animals, or
(b) placed in a shelter) for the animals.
The farmer is obliged to pay the costs incurred for the care of trapped
an animal in a shelter for the animals.
(6) the implementing legislation provides for the Organization, the content and the conditions
vocational course for the capture of stray and abandoned animals and their treatment
them, including care in animal shelters for animals, and for the collection and destruction of
disposal of animal carcases in pet food, as well as the organisation and
the contents of the final exam.
TITLE VI OF THE
STATE ADMINISTRATION IN MATTERS OF ANIMAL HEALTH CARE
§ 43
Government authorities in matters of animal health care
The State administration in matters of veterinary care, exercise
and) the Ministry,
b) Ministry of defence and Ministry of the Interior,
(c)) community,
d) veterinary authorities.
§ 44
(1) the Ministry of
a) provides for guidelines development and tasks of veterinary care and checks
their fulfilment,
(b)) the exercise of State administration in matters of veterinary care and decides on
appeals against the decisions of the Central Veterinary Administration,
may declare any geographical area for the region affected by the Special
geographic constraints;
(c) approves the programs to repair the animals) and the guidelines for preparing
contingency plans and exposes them in the journal of the Department of
Agriculture and on their website,
(d)) on the basis of the health situation and its anticipated development and is
taking into account the special health guarantees required in connection with
international trade in animals and their products, lays down that
programs to reviving animals, acts related to the control of the inheritance
health, operations relating to the control of animal welfare, compulsory
preventive and diagnostic actions to prevent the emergence and spread of diseases and
diseases transmissible from animals to humans, as well as to their control,
be carried out in the calendar year, including the conditions and time limits for
their design, exposes their list in the Gazette of the Ministry of
Agriculture and on their website, and determines which of them
and to what extent they are to be paid from the funds of the State budget. Between
diseases covered by these acts are always tuberculosis, brucellosis
and enzootic bovine leukosis, as well as brucellosis and Aujeszky's disease
pigs,
e) coordinates the activities of Central Government authorities in the performance of tasks
related to the prevention of the emergence and spread of dangerous diseases and
their meeting,
f) may change or terminate the emergency veterinary measures proclaimed
The Central Veterinary Administration, lasting longer than 15 days,
g) decides on compensation for costs and losses incurred in connection with
dangerous diseases.
(2) the Ministry shall set up the State Veterinary institutes and the Institute for
scientific research activities in the field of veterinary medicine and the proposal
The State Veterinary Administration approved national reference laboratories;
the list of national reference laboratories, shall be published in the journal of the
The Ministry of agriculture.
(3) the Minister of agriculture shall be established in agreement with the central authorities of the State
Administration, accounting for some of the tasks related to the prevention of the occurrence and
the spread of dangerous diseases and their control, Central Health
the Commission as a permanent advisory body.
§ 45
(1) the Ministry of defence and Ministry of the Interior in the scope of its competence
and implementation of the emergency) animal health measures ordered
other authorities, as appropriate, in agreement with the authorities of your own
emergency veterinary measures,
(b)) carried out in cooperation with the State Veterinary Administration of the mandatory
preventive, diagnostic and therapeutic actions to prevent the emergence and spread of
dangerous infections and their control, as well as other technical support
Veterinary acts needed to health and veterinary inspection of inheritance
health,
(c) shall be exercised by the State veterinary supervision) and takes measures to eliminate
any identified deficiencies, and that the Ministry of defence in the important
for the defense of the State of ^ 24a) and the Ministry of the Interior in establishments
managed in conjunction with the fulfilment of their tasks,
(d)) provides the State Veterinary Administration information of importance for the
the prevention of the emergence and spread of dangerous diseases and health care
the safety of animal products.
(2) Veterinary doctors the Ministry of defence and the Ministry of the Interior,
where appropriate, they have established organizational units of the State, who were
entrusted with this activity,
and they expose the passports of dogs) used by these ministries to carry out their
tasks, if these dogs are transported between Member States
non-commercial purposes, and taken them to perform serological samples
a test certifying rabies antibody titer and the
b) carry out checks of dogs used by these ministries to carry out
their task at the entrance of these dogs from third countries at points of entry
According to the article. 10, paragraph 1. 2 of the European Union concerning animal health conditions
for the non-commercial movement of pet animals ^ 48) intended
The Ministry of Defense or the Ministry of the Interior.
(3) the veterinary doctors medical certificate shall be issued by the Department of Defense
for animals not kept in buildings important for the defence of the State.
§ 46
The municipality
and) endorses the points at which markets can be held for resale of animals and
animal products (market hall and market square) and after determination of veterinary
the conditions of the places where you can take place leads to animals, and permits the holding of
these markets and standpipes. On the territory of the city of Prague approved these places
and to permit the holding of these markets and the lure of the city district of the capital city
Prague,
(b) on a proposal from the County) is issued by the Veterinary Administration of the regulation of the village) on the 25 ^ ^
Regulation of the emergency veterinary measures terminating the extraordinary
veterinary measures and oversees their implementation. However, this does not apply to
the city of Prague, in which he announces and terminating the emergency veterinary
always measure the city animal health management in Prague,
(c)) alone or in cooperation with other municipalities or other person may set up and
operate a shelter for animals harvested pursuant to § 42 para. 1,
(d)), the costs associated with the catching and karanténováním odchyceného
the animal under section 42 unless the breeder I know,
e) participates in its territory, which extends into the protection zone, zone
surveillance or further restricted zone, on the assurance of the
emergency veterinary measures ordered by the State Veterinary
the Administration, in the manner and to the extent laid down by these measures; on
the territory of the city of Prague is to support the above measures
involved in the urban part of the city of Prague. For the reimbursement of costs and
losses incurred by the municipality and in the case of the city of Prague city district in
delivering emergency veterinary measures
Similarly, section 67 para. 2, § 68 para. 1 and § 70 para. 1 and 2.
§ 47
Veterinary authorities
(1) the authority of the State Veterinary Administration of the veterinary service and the administrative
Office with statewide jurisdiction subordinate the Ministry of agriculture
(hereinafter referred to as "the Ministry").
(2) the State Veterinary Administration is the business component of the State and the Court of
unit. Its capital is Prague.
(3) the Institute for State control of veterinary Biologicals and medicaments (
"the Institute") is a body of the veterinary service for the area of veterinary
preparations and veterinary technical resources, organizational component
the State and the entity.
(4) the State Veterinary Administration is made up of the Central Veterinary Administration,
the regional veterinary administrations carrying out its activities in the
matters of veterinary services in the territory, which is identical with the territory of the regions referred to in
another law ^ 7a), and urban veterinary services in Prague, which
the scope of the regional Veterinary Administration shall exercise within the territory of the capital
Prague.
(5) at the head of the State Veterinary Administration is the Central Executive, which controls
The Central Veterinary Administration; his selection, appointment and removal shall be governed by
the law on the civil service. The selection, appointment and dismissal of the Director of the regional
the veterinary service is governed by the civil service.
(6) the Central Director appoints and dismisses, with the consent of the Minister
Agriculture, Director of the State Veterinary institutes.
(7) the scope of the State Veterinary Administration shall be exercised by the Central
the veterinary services and the regional veterinary administrations. As the authority
the first instance in administrative proceedings shall be decided by the regional Veterinary Administration
According to its territorial jurisdiction, the appeal against the decision of the regional
Veterinary Administration shall be decided by the Central Veterinary Administration, with the exception of §
48 para. 1 (b). (f)), g), (l)), and p), in which it shall act as the authority
the first degree of the Central Veterinary Administration.
§ 48
the title launched
(1) the Central Veterinary Administration
and the concept of health protection) handles the animals and care about health
the safety of animal products, multi-annual control plans in order to
regularly verify compliance with legislation relating to
the health and well-being of animals and the health of animal products and
feed monitoring plans of certain substances and residues thereof and secures the
the implementation of these concepts and plans,
(b) be submitted to the Ministry for approval) proposals for programmes to repair
animals, including proposals for funding, and ensures their
implementation of policy proposals, for drawing up the contingency plans, as well as, in the
the case of livestock, after consultation with the agrarian Chamber, proposals for
the determination of the additional mandatory preventive and diagnostic operations to
the prevention of the emergence and spread of diseases and diseases transmissible from animals to
humans and their control that are not listed in § 44 para. 1 (b).
(d) the second sentence). Upon occurrence of emergency situations organizes activities
the crisis centre disease control ^ 25b)
(c)) shall draw up and update the national contingency plans, coordinates
the implementation of the compulsory preventive and diagnostic operations to prevent
the emergence and spread of diseases and diseases transmissible from animals to man and to the
their control, shall decide on the regulation, amendment and termination of the emergency
veterinary measures and oversees their implementation, he admits, be suspended
and restores the present economy and the status of the areas free of the disease, leads
a list of them and proposed to the authorities of the European Union to the Czech Republic
granted the territory of the free area,
(d)) governed by the regional Veterinary Administration, decides on appeals
against their decision and against decisions of the Institute,
(e)) of the Constitution and governed by the State Veterinary Institute and coordinates their training
activity, proposes to the Ministry for approval to the national reference
laboratory and approved reference laboratories, directs and coordinates the
their activities,
(f) shall be exercised by the State veterinary supervision) and issued binding guidelines to
the deficiencies, shall carry out official controls and audits, and the
based on their results shall take appropriate measures, in accordance with the
European Union legislation to soften the exceptions from the veterinary and
health requirements laid down in the animal health and welfare, on
animal products, as well as to the construction, layout and equipment of
undertakings, businesses, and other devices, in which the animal is treated
products and animal by-products, for these exceptions
national nature or relate to the territory of several counties
(g) issuing binding opinions) in cases in which the issue of
reserves, in terms of health gives consent to the biological
testing so far unused feed, their production, imports and entry into
circulation, specifies the cases in which you need to perform specific evaluations
the efficacy of the biocidal products against established designers of diseases,
h) performs checks according to the Act on the State agricultural intervention
the Fund for the purposes of this Fund,
I) examines whether a border veterinary station meets the requirements for
location, material and personnel equipment veterinary station
border controls, suspended its activities, in particular if required
protection of human and animal health, on request, the importers of animals or
animal products, for which import conditions have been established
(harmonized) at the level of the European Union, tells the import conditions
applicable to imports of animals or animal products of the species from
the third country or part thereof to the United States and determines which
vaccination is preventing the importation of animals and their products may, in connection with the
tasks relating to border veterinary checks on request from
the Customs authorities the information necessary in terms of management and international
cooperation in the field of this check,
j) leads, updates and publishes on the website of the State
Veterinary Administration lists of approved and registered, or
the allowed
1. the participants in the network monitor, assembly centres, quarantine
centres, semen collection centres, semen collection centres, banks
semen, livestock equipment, including breeding animals
the aquaculture and other devices involved in
the circulation and marketing of animals on trafficking,
2. undertakings, businesses, or other devices involved in
production, processing and marketing of livestock products into circulation and the
trading with them,
3. persons as entrepreneurs ^ 10) transporting animals or animal
products and are subject to registration, as well as the traders referred to in § 9b,
4. third countries or parts thereof from which the animals may be imported
or animal products into the United States,
5. undertakings, and/or other equipment in third countries, from which you can
Importing animal products into the United States,
6. veterinary laboratories, rendering undertakings and other persons
they perform some of the rendering activities referred to in § 39 para. 1,
7. free zones, free warehouses and customs warehouses
under veterinary supervision,
8. other persons, enterprises, factories, and other facilities and centres
the funds, if they have been approved and registered,
registration required by this Act or the regulations of the European Union;
the lists referred to in points 1 to 8, transmitted to the Commission and the other Member States,
If required by the regulations of the European Union,
k) published on the website of the State Veterinary Administration
accordance with the legal acts of the European Union models of veterinary certificates,
as well as lists of the European Union reference laboratories, the national
reference laboratories in the Member States and the laboratories of the Member States
authorized to perform specific laboratory activities, if it acts
The European Union requires,
l) issues, changing and withdrawing the natural and legal persons the authorisation
1. for the implementation of laboratory or other veterinary diagnostic
the activities, for which the results are to be used for the purposes of the State
veterinary supervision,
2. for the operation of the undertaking, the rendering
m) collects, processes and evaluates information from the field
veterinary care including data Czech Republic undertook to submit
international organisations due to their membership, leads,
operates and develops the information system in the field of health care in
accordance with the specific legislation ^ 25 c), working with administrators
other information systems that are used for the performance of public administration in the Czech
Republic and secures the functional integration of the information system in the
the field of veterinary care in international information systems
the field of veterinary care,
n) organizes the content of study of official veterinarians and grants
attestation, organizes professional training of veterinary assistants,
organizes training courses and further training of employees of the State
Veterinary Administration,
about) works
1. with the agrarian Chamber of the Chamber of Commerce, food, and other
professional interest associations, as well as with the veterinary and pharmaceutical
University of Brno in matters relating to their scope and
of common interest,
2. the institutions of the European Union, which administered the required by them or the regulations
The European Union provided for information, news, opinions and papers in the field of
its scope, and with the Member States, which provides the necessary
cooperation, in particular the information set out the rules of the European Union,
3. foreign veterinary services and relevant international
organisations,
p) perform the tasks arising for it from the immediate binding legal
European Union legislation ^ 2), and in particular shall be supervised over the exercise of
the obligations arising for the natural and legal persons of the
European Union legislation ^ 2), issue a permit to the adoption of secondary
animal products belonging between materials 1. or 2. the categories and
processed products derived from those materials that are
sent from other Member States to the United Kingdom as a State
determine, in the case of cross-border cooperation carried out surveillance and progresses
According to the regulation of the European Union relating to cooperation in the field of
consumer protection ^ 25 d), and in the case of illegal
hearing ^ 25e), which controlled a person committed in the territory of the European
the European Union or in another State the stand of the European economic area and which
harms or may harm the common interest of consumers ^ 25f)
by a decision of such conduct disables, q) shall determine at the request of the authority
the executing State supervision pursuant to the Act on the Czech commercial inspection, ^ 25 g)
or the law on the customs administration of the Czech Republic ^ 25 h), that the State
the Veterinary Institute carried out laboratory tests to identify the
species in accordance with the European Union, which prohibits the
placing on the market, import to or export from the community of cat and dog
fur and products containing such fur ^ 25i CKS),
r) gives producers passports a series of numbers in accordance with art. 21, art. 3
Regulation of the European Union concerning animal health conditions for non-commercial
movements of pet animals ^ 48),
with other tasks) established by this Act or by a specific legislative
^ 1b) regulations.
(2) Implementing law provides specific requirements for equipment,
the method and organization of the operation of information system in the field of veterinary
care.
§ 48a
(1) the Central Veterinary Administration informs the public on the basis of the results of the
the State veterinary supervision of animal products,
that are not wholesome, or animal products
unfit for human consumption in accordance with art. 10 of regulation of the European
Parliament and of the Council (EC) No 178/2002.
(2) the Central Veterinary Administration is entitled to inform the public on the
based on the results of the State veterinary supervision of
and) discovered animal products labelled or offered
misleading terms, or
(b) confirm the presence of a dangerous disease), or diseases transmitted from animals
for a man that can endanger the health of humans or animals.
(3) Public Information published in accordance with paragraphs 1 and 2 may
contain the identity of the controlled person, the nature of the risk,
the measures taken and any other information necessary to protect the health of people and the
animals. These cases are not covered by the obligation of confidentiality of the stored
under special legislation ^ 51).
§ 49
The regional Veterinary Administration
(1) the regional animal health management
and draws up and updates) in accordance with the national emergency
plans for the regional contingency plans and monitor their implementation, organizes
the activities of the regional crisis centre disease control ^ 25b)
(b) the implementation of the compulsory preventive) and diagnostic tasks
to prevent the emergence and spread of diseases and their control, approve and in the
the case of non-execution provided for compulsory preventive and
diagnostic operations [§ 5 para. 1 (a)), § 44 para. 1 (b). (d))]
suspending or withdrawing the status of the holding officially free
dangerous infections, approved the healing programs, approved breeders
area intended for cleaning and disinfecting means of transport
used for the carriage of animals and fulfil the tasks arising for it from the schedule
the monitoring of certain substances and residues thereof,
c) decide on the regulation, amendment and termination of the emergency veterinary
measures within the jurisdiction of the county or any part thereof, in excess of the territorial perimeter of the village,
keeping a watch on their performance, and allow individual exceptions to the ordered
emergency veterinary measures,
d) decide on the regulation, amendment and termination of the emergency veterinary
the measures, which impose obligations individually determined by the physical and
legal persons, and oversees their implementation,
e) announces the results of the preliminary examination of animals suspected
of the occurrence of a dangerous disease Central Veterinary Administration and after their
the confirmation of the occurrence of this disease to the competent regional authority, village, on
the territory of the city of Prague municipal parts of the capital city of Prague, the authority
Police of the Czech Republic and the locally competent authority Chamber of Commerce, the incidence of
diseases transmitted from animals to humans also to the competent authority of the protection
public health,
(f)) of the disease reasons, may order the owner, to the animal to
Veterinary examination, protective vaccination or to perform another
the professional of the Health Act, and specifies the conditions and duration of the
quarantine and isolation,
g) carries out the State veterinary supervision and issued binding guidelines to
the deficiencies, carries out a planned official controls,
checks in the event of a suspected non-compliance with the obligations and requirements and
audits, and on the basis of their results shall take appropriate measures, validates the
compliance with the specifications according to the regulations of the European Union on agricultural
products and foodstuffs as traditional specialities guaranteed,
and on the protection of geographical indications and designations of origin for agricultural
products and foodstuffs ^ 25j), as regards the products and foodstuffs of animal
of origin, be authorised in accordance with the regulations of the European Union to soften the exceptions
for animal health and public health requirements laid down in the animal health and
their well-being, to animal products, as well as to the construction, layout
and equipment of enterprises, plants and other facilities in which is treated with
animal products, animal by-products and, if
the authorisation of these exceptions is not the Central Veterinary Administration,
h) approve and registers, registers in the
the scope of the
1. the participants of the network monitoring, assembly centres, quarantine
centres, semen collection centres, semen collection centres, banks
semen, livestock equipment, including breeding animals
the aquaculture and other equipment involved in the marketing of
animals of the circulation and trafficking,
2. businesses, factories or other facilities involved in the production,
processing and marketing of livestock products into circulation and trading
them,
3. persons as entrepreneurs ^ 10) transporting animals or animal
products and are subject to registration, as well as the traders referred to in § 9b,
4. the rendering undertakings and other persons carrying out just a few of the rendering
the activities referred to in § 39 para. 1,
5. private veterinary surgeons for assembly centres or for the
certain activities if their approval required by this Act or
regulations of the European Union,
6. free zones, free warehouses and customs warehouses under
the State veterinary supervision,
7. other persons, enterprises, factories, and other facilities and centers
means, if their approval and registration,
registration required by this Act or the regulations of the European Union; withdrawing the
or suspend the approval and registration, or cancels the registration,
the conditions are met for such measures provided for by this Act
or the regulations of the European Union,
I) issued binding opinions for construction management, construction, and announcements for
occupancy and certifies compliance with the requirements and conditions laid down
for the treatment of animal products,
j) applies its opinions on the territorial plans, regulatory plans and binding
the opinion of the territorial management in terms of health care,
to) specifies the animal health conditions for animals and animal health lead
the conditions for carrying out experiments on animals, registers the circuses, releases
registers of circus animals and indexes of performance
circuses, confirms the passports for circus animals, performs checks
compliance with the obligations and requirements associated with the movement of the circus
animals between Member States and verifies that the conditions are met to
the relocation of the circus from the United Kingdom to other Member States,
l) a person who manufactures, processes, imports, treats, stores,
transports, puts into circulation and uses the feedingstuffs of animal origin, specifies the
the animal health conditions for their use so as to avoid their
actors adversely affected their health
wholesomeness. For feedingstuffs which have been treated with substances harmful to human health
or otherwise adversely affecting animals or animal products
or to which such substances have been added in accordance with the approved
technological procedure and which, therefore, can be used to feed only
After the expiry of the withdrawal period, if necessary, be determined in this
a time limit or other health conditions and measures and checks their
compliance with,
m) issued after the veterinary inspection veterinary certificates and
responsible for its completeness and correctness,
n) performs the inspection of slaughter animals and meat, as well as veterinary
examination of other animal products and assesses their applicability
(edibility), issued to the operators of poultry or rabbit slaughterhouses
authorization to perform certain operations in the context of meat of poultry and tours
Lagomorphs own staff and decides on the amount of the reimbursement of costs
associated with the performance of this tour explores the own-checks system
the hygiene conditions of production of entrepreneurs ^ 10) referred to in section 22,
approves the contingency plans operators of slaughterhouses, traffic and sanitation
schedules referred to in § 22 para. 1 (b). (b)) (3) gives and takes away the consent to
the sale of small quantities of raw milk farmer in the place of manufacture or
through the vending machine directly to the consumer,
about performs veterinary control) animals and animal products
are subject, in the place of their origin, in the course of their
transport or at their arrival at the place of destination, and if it is part of the
the regional Veterinary Administration border veterinary station, also
border veterinary inspection of controlled goods imported from
third countries; in the context of the implementation of the border veterinary
checks may request from the Customs authorities the information necessary for the proper
the performance of this check,
p) adopt appropriate measures, if they are not
1. met the animal health conditions laid down in this Act or the regulations
The European Union for trade in animals and animal products, or
for the import of animals and animal products,
2. compliance with obligations or requirements established by this Act, or
European Union regulations for assembly centres, or
3. compliance with obligations or requirements laid down by a regulation of the European
the Union, which prohibits the placing on the market, imported into the community and
to export from the cat and dog fur and products containing such fur ^ 25i CKS),
in the case of cat and dog fur in the rough,
q) if required by the performance of the State veterinary supervision, performs
animal health prosektorskou activities in the rendering undertakings,
r) registers the graduates of professional schools for the veterinary field,
where appropriate, the graduates of post-secondary studies veterinary field who
are entitled to some expert veterinary acts
the business way, (hereinafter referred to as "private veterinary technician")
with the changes, and releases) takes away natural and legal persons the authorisation
1. for the implementation of laboratory or other veterinary diagnostic
activities for the purpose of examination for trichinae of wild game,
(Trichinella), unless an authorization to perform laboratory or
other veterinary diagnostic tasks, the results of which are to be
used for the purposes of the State veterinary supervision,
2. the performance of some veterinary rendering activities (section 51 (1)),
unless the operation of the undertaking, the rendering
3. for the implementation of home defeats of bovine animals under 24 months or
from a farmed deer breeding in the holding of the keeper,
4. the slaughter of farmed game at the farm, to kill the big
farmed game meat in the economy by the use of firearms or to your home
the slaughter of farmed Deer farming by the use of firearms,
t) performs checks of cross-compliance under the law on agriculture ^ 25 l)
accordance with the EU regulation governing the detailed rules for the
cross-compliance, modulation and the integrated administration and control
^ 25 m), the system performs checks according to the Act on the State farm
the intervention fund for the purposes of this Fund, and issue certificates for
the provision of special export refunds,
u) stores the fines for non-compliance with or breach of the obligations, requirements or
conditions laid down in this Act and the regulations of the European Union,
perform the tasks resulting in) for it from immediately binding legal
European Union legislation ^ 2), and in particular shall be supervised over the exercise of
the obligations arising for the natural and legal persons of the
European Union legislation ^ 2), carried out in the case of cross-border cooperation
supervision and proceed according to the regulation of the European Union relating to the
cooperation in the field of consumer protection ^ 25 d), and in the case of detection of
infringement ^ 25e), which is controlled by the person committed to the
the territory of the European Union or in another State, representing the European economic
space and which harms or may harm the common interest
consumers ^ 25f), disables such behaviour, decision
x) fulfil such other tasks provided for in this Act or special legal
^ 1b) regulations.
(2) the Director of the regional Veterinary Administration establishes the Health Commission, which
It is an advisory body.
(3) the part of the County's Emergency Center Veterinary Administration for
the emergency situation, which, in accordance with national emergency plans
intervenes in the outbreaks of diseases and other emergencies.
§ 49a
(1) the State Veterinary Administration
and) based on a duly substantiated request by the competent authority of the Member
State (hereinafter referred to as "the applicant authority")
1. the applicant authority shall forward the information, news, opinions, papers
or certified copies thereof, or briefs and documents (
"information and documentation") which has or may
obtain and verify that enable compliance with legislation on
veterinary care. When obtaining such information and documents
they can be supplied also in electronic form, it shall State
animal health management as if filled custom tasks or acted on
the request of an authority of the Czech Republic,
2. examine the accuracy of the facts in an appropriate manner, it
notified to the applicant authority and inform it of the results of the screening exercise,
including the information that was necessary to examine the
3. it shall inform the applicant authority of the administrative decisions or other
acts relating to the application of legislation on veterinary care,
4. carry out or strengthen State veterinary supervision within its scope of
where there is a suspected breach of the legislation, in particular
supervision of businesses, places where stocks of goods have, of which the
movements of goods and means of transport,
5. the applicant authority shall provide all relevant information that has
available or which it obtains in accordance with point 1, a real
meetings or practices, which are based on the requesting authority in violation of the
legislation on veterinary care,
(b)), even without the application if it considers it appropriate,
1. carry out or strengthen State veterinary supervision at locations listed
under (a), point 4)
2. provides the competent authorities of the Member States as soon as available
the information and documents which relate to acts or practices that are in the
or appear to be contrary to legislation on veterinary
care, in particular as regards the methods or methods used in these
activities.
(2) the request for information, in which the subject matter of the administrative decision
or any other Act, the disclosure of which is sought, must be provided with
translation into the Czech language.
(3) the State Veterinary Administration shall inform without delay the Commission with all the necessary
information relating to the
and) goods which are the subject of, or suspected, that is
subject to the acts or practices that are in conflict with the law
about veterinary care,
b) methods and procedures that are being used, or where there is a
believing that they are being used in violation of the legislation on
veterinary care,
c) shortcomings or gaps in the legislation on veterinary care,
that are detected in the application of these provisions.
(4) if the information provided of cases which may
constitute a danger to human health, which cannot otherwise be avoided,
This information may be, upon agreement between the involved authorities and the Commission
communicated with the reasons to the public.
(5) The mutual assistance referred to in paragraphs 1 and 3 cannot be provided,
If this would be contrary to the legal regulations of the Czech Republic,
or if it would prejudice the public policy or other essential
interest in the United States. Information and documents relating to the physical or
legal entities may be provided only to the extent strictly necessary to
notice of meetings or practices which are inconsistent with the law of
veterinary care. Any refusal of assistance must be justified.
(6) the information provided in any form to the competent authorities are
of a confidential nature; their provision is covered by the obligation of
discretion and is subject to specific legislation. The competent authorities of
shall ensure that the information provided remains confidential, even after the conclusion of the
case. This information can be used in the event of litigation or
proceedings instituted for failure of the legislation on animal health
care, or in preventing and detecting deficiencies in relation to the funds
Of the European Union; such use of the information provided must be
the competent authority shall be informed of the Member State that provided the information.
(7) information under this provision may not be provided to other
persons other than those whose duties in other Member States or in
bodies of the European Union, require, in order to have access to this information.
This information may not be used for purposes other than those
laid down by that provision, unless the authority that information
It Express consent and unless such communication or use
the information is not contrary to the legislation of the Member State in which is situated
the authority has received the information.
(8) if the State Veterinary Administration learns about the negotiations or
procedures, which are, or appear to be contrary to the legal
provisions on veterinary care, especially if they are related or are likely to
also apply to other Member States, it shall inform the Commission of its own
initiative or on the basis of the substantiated request; If necessary, it
will also provide the necessary information and documents. The State Veterinary Administration
shall inform the Commission and the other Member States of bilateral agreements
on mutual assistance concluded with the competent veterinary authorities
third countries.
(9) with the exception of payment of fees paid to experts with assistance under
This provision provides, free of charge.
(10) this provision shall not affect the regulations on mutual legal
assistance in criminal matters.
Authorization to pursue certain professional veterinary activities
§ 50
(1) the Central Veterinary Administration may issue a permit to the implementation
Laboratory, or other veterinary diagnostic activities, the
the results will be used for the purposes of the State veterinary supervision,
a person who has reached the age of 18 years has the capacity to perform legal acts, is
integrity, for the performance of the activities of the competent and
exercise in an environment and under the animal health and hygiene conditions, which
According to the observations correspond to the appropriate regional veterinary administration of the nature and
the range of appropriate activities.
(2) the Central Veterinary Administration shall issue a permit to operate a rendering
business person who fulfils the conditions set out in paragraph 1.
(3) the regional Veterinary Administration may issue a permit to the implementation
Laboratory, or other veterinary diagnostic activities to
examination of wild game on the trichinae (Trichinella), unless the
authorization to perform laboratory or other veterinary
diagnostic activities, the results of which will be used for the purposes of
the State veterinary supervision, to a person who has reached the age of 18 years, has
competence to perform legal acts, is unexceptionable, to exercise that activity,
competent and will perform in the environment and under the animal health and
hygiene conditions conforming to the type and scope of such activities.
(4) in the case of a legal person, the conditions set out in paragraphs 1
and 3 meet its professional representative. If it is a person that has not yet been
assigned the identification number of the person, gives it a regional animal health
identification number of the management person at the same time with the issue of a permit under
paragraphs 1 to 3; the identification number of the person the basic administrator
the registry of legal persons, natural persons-entrepreneurs and authorities
public authority (hereinafter referred to as "the register") ^ 39).
(5) For integrity, for the purposes of this Act shall be considered one who is not
convicted in the last 10 years for an intentional crime
or in the last 5 years for an offense committed by negligence in the
connection with the professional veterinary activities. In order to demonstrate
integrity of the competent authority referred to in paragraphs 1 to 3 shall request
under special legislation ^ 25 g) extract from the register Index
the sentencing guidelines. An application for a statement of convictions and an extract from the
criminal records shall be transmitted in electronic form,
manner allowing remote access.
(6) must be specified in the permit, the nature and scope of activities and the professional
Representative, and in the case of the rendering undertaking, whether or not the territorial circuit in which
the activities carried out, (the purpose of the area).
(7) the Central Veterinary Administration or regional Veterinary Administration may
to change or withdraw the authorisation issued to her, if the activity is not
exercised in accordance with the law or have changed the conditions under
which the authorisation was granted.
(8) laboratory, where appropriate, other veterinary diagnostic activities
the purpose of the examination of wild game on the trichinae (Trichinella), unless the
authorization to perform laboratory or other veterinary
diagnostic activities, the results of which will be used for the purposes of
the State veterinary supervision pursuant to the provisions of paragraph 3 shall be entitled to
to carry out the veterinarian, veterinary technician, private person
competent pursuant to section 59A(1). 1 (b). b) to (e)), or
a person who graduated from a specialized professional training, with a focus
the investigation game on trichinae (Trichinella), has passed the
final exam and a certificate of eligibility to this
activity.
(9) a specialized professional training with a focus on investigating
game on trichinae (Trichinella) organizes high school with
the health curriculum, which is issued by persons who
This specialized professional training completed, a certificate of
eligibility for the investigation of wild game meat for trichinae (Trichinella)
keep a list of these people.
(10) the detailed legislation lays down the content, scope and organization of the
specialized training focusing on the investigation into the game on
trichinae (Trichinella), method and organization validation
acquired knowledge, certification and maintenance of a list of persons who
This specialized professional training undergone.
§ 51
(1) the regional Veterinary Administration shall issue a permit unless the permit to
the operation of rendering the undertaking (section 50 (2)), for the performance of some of the
Veterinary rendering activities referred to in § 39 para. 1 person
satisfies the conditions laid down in this law and the regulations of the European Union
governing health rules for animal by-products which
they are not intended for human consumption ^ 9b). In the case of capture of stray or
abandoned animals or of the collection and disposal of animal carcases in
pet, this must be by a competent person in accordance with §
paragraph 42. 2. for the amendment or withdrawal of an authorisation shall apply mutatis mutandis to § 50 para.
7.
(2) the authorization shall be determined by the nature and scope of activities, and in the case of collection and
disposal of animal by-products, also the place where
These products will be harmlessly removed or further processed.
In the case of an authorisation to a person, that have not yet been allocated
the identification number of the person, gives it a regional animal health management
the identification number of the person at the same time with the issue of the permit referred to in paragraph 1;
the identification number of the person shall provide the registry administrator people ^ 39).
(3) Regional animal health management checks in the exercise of State
in particular, the veterinary supervision of compliance with the requirements of this
the activities provided for in this law and the regulations of the European Union ^ 9b).
§ 51a
The national reference laboratories and reference laboratories
(1) the Ministry of approved national reference laboratories for the purpose of
deepening coordination and unification of laboratory and diagnostic
activity; approval may withdraw it if the activity is not exercised
properly, or if you have changed the conditions under which the authorisation.
(2) the Central Veterinary Administration approved reference laboratories for
the area of health care, and for the activities for which they have not been
the Ministry approved the national reference laboratory. For reference
paragraph 1 shall apply, mutatis mutandis, of the laboratory.
(3) Implementing legislation sets out the requirements for the material and
personnel facilities the national reference laboratories and reference
laboratories and on focus, organization, and methods of their activities.
The State veterinary supervision
§ 52
(1) the veterinary authorities carry out the State veterinary supervision in
accordance with this law, special legislation and regulations ^ 25 h)
The European Union ^ 40). When its performance
and) shall keep, for compliance with the obligations, requirements and conditions
established by this Act, special legislation ^ 25 h) or
European Union regulations or on the basis thereof and in which they laid down
limits, and finding weaknesses, their causes and the persons responsible for them,
b) discuss and if necessary impose mandatory guidelines, which
and in what period of time they are to be removed and identified deficiencies
control their implementation,
c) monitor the health situation in the environment of wild animals.
(2) Specific forms of State veterinary supervision are veterinary
health check and health check for inheritance of marking and registration
animals, veterinary health inspection of feedingstuffs, inspection
of slaughter animals and meat, the border veterinary checks and animal health
check on arrival at destination.
(3) if the basis for the decision of the Veterinary Administration of the result
laboratory examination of samples, must be the result of the examination
carried out by the
and the State Veterinary Institute), the national reference laboratories,
reference laboratory or a laboratory that has been issued for the appropriate
heading the investigation certificate of accreditation under the law on technical
requirements for products ^ 17 k) and that of the Central Veterinary Administration has issued a
authorisation to carry out veterinary laboratory and diagnostic activities
(b)) other body of State supervision laboratories that performs laboratory
examination of samples for official controls, or
(c)), the European Union's reference laboratory or by a laboratory in another Member
State approved for carrying out the laboratory tests on the samples in the
official controls.
(4) when the laboratory examination of samples shall be treated according to the standards and methods
established on the basis of the legislation of the European Union ^ 41).
(5) for the performance of the State veterinary supervision of the Ministry of defence and
The Ministry of Interior, the provisions of paragraphs 1 to 4 apply mutatis mutandis.
§ 53
(1) the official veterinarians of the veterinary and veterinary management
doctors of the Department of Defense and the Ministry of the Interior, where appropriate, by
set up by organisational units of the State delegation of the State
veterinary supervision (hereinafter referred to as "health inspector"), shall be entitled to
During his performance,
and invalidate) in place of animal products that are not disabled
safe, or to order their deterioration and destruction, and
on the load controlled person
(b)) to suspend, restrict or prohibit the manufacture, processing or marketing
animal products into circulation, if the conditions are not met, and
the requirements established by this Act, special legislation ^ 26)
or the regulations of the European Union ^ 47) on animal products and handling
them,
c) suspend manufacture, processing or marketing of animal products into the
circulation on the reasonable period of time on suspicion that they are not wholesome.
(2) the regional veterinary administration ends
and the stored measures) pursuant to paragraph 1. (b)), if it was a defective condition
removed,
(b)) the measures imposed under paragraph 1 (b). (c)), if the controlled person
It proves that animal products are wholesome.
(3) the animal health inspectors are required to
and to prove the credentials to check) under the inspection order ^ 43) staff
identification,
(b)) Protocol on measures taken pursuant to paragraph 1.
(4) for the official veterinary assistants shall apply mutatis mutandis in paragraph 3 and the rights and
the obligations laid down by the inspection regulations controlling ^ 44).
(5) in the samples taken shall be granted a refund, with the exception of samples
taken on the sale of foodstuffs of animal origin in accordance with special
^ 28) legislation, for which the controlled person will provide
substitute ^ 27), if you ask for it within 6 months from the date on which the
acquainted with the fact that the food complies with the requirements laid down
special legislation ^ 28). The refund shall be controlled by the person
shall, within 30 days of the date when asked about her.
(6) the implementing legislation provides for
and animal health aspects) for the determination of the frequency of official controls and
audits, if their frequency is not regulated in the European Union,
(b)) how to monitor the animal health situation in the environment of wild animals,
(c) the service card) model of the veterinary inspector and official
the veterinary assistant.
(7) where the Commission implements its experts, where appropriate, experts from other
the Member States, who are included in a list maintained by the Commission for these
the purpose, in collaboration with the veterinary authorities for checking compliance with and
uniform application of the duties and requirements laid down in this
the law and its implementing legislation, or the rules of the European Union,
on location in the Czech Republic, veterinary authorities provide them with
the support that they need to complete their task.
(8) For carrying out the checks referred to in paragraph 7, the provisions
paragraph 3 (b). and) and the rights and obligations provided for by the controlling
the inspection regulations ^ 45) apply mutatis mutandis. In particular, it must be referred to specialists
given the same access to sites, facilities and means of transport, which
have veterinary inspectors. The information collected referred to experts in the
during checks and conclusions from them must not be used under any circumstances
for personal purposes or divulged to persons who do not belong to the relevant
departments of the Commission or the Member States.
§ 53a
State supervision over the classification of the carcases of animals for slaughter
(1) State supervision over compliance with the obligations laid down by the law on
foodstuffs shall be exercised by the veterinary inspector.
(2) State supervision over the implementation of the classification of carcasses
slaughter animals according to the law on foodstuffs and the person may exercise the
that is not a health inspector (hereinafter referred to as "the Inspector").
(3) inspectors shall apply mutatis mutandis to the rights and obligations of controlling
set out the inspection regulations ^ 46) and section 53 para. 3 (b). and Detailed).
the legislation lays down the model of professional licence Inspector.
(4) an inspector may, with the written mandate of the Central Director
to exercise State supervision over the implementation of the classification of carcases
the bodies of animals for slaughter, even outside the territorial scope of the regional animal health
the Administration, of which he is an inspector. In proceedings on administrative offence detected
during the inspection, during which the Inspector has progressed in the first sentence, shall be decided by
as the authority of first instance regional Veterinary Administration, in whose territorial
the circuit has been checked.
Emergency veterinary measures
§ 54
(1) Emergency veterinary measures are
and veterinary diagnosis and regulation), the vaccination of animals,
(b)) the definition of the outbreak, the protection and surveillance zones, warning
indicate, where appropriate, the guarding of the outbreak,
(c) the quarantine regulation or separate) location (isolation), or
need to slaughter or killing of animals,
d) restriction or prohibition on the movement, sale, trading, free
movement, slaughter and breeding animals, and conduct experiments on animals,
e) restriction or prohibition of grazing, the use of sources of water and feed,
f) restriction or prohibition of holding leads, capture the animals, hunting game and hunting
fish,
g) limit or ban the sale of animals and animal products in markets
and on the markets or the conclusion of the market or the marketplace,
h) suspension of handling of animal products and feed into the
the end of the required examination, regulation of separate storage (storage)
medically harmful or suspect animal products or animal feed,
I) restriction or prohibition of the manufacture, processing, transport and marketing of the
circulation disabled bad or suspect animal products or
feedingstuffs, the specific conditions for their production, processing and
the carriage or the regulation of their destruction,
j) determining the special conditions, including its limitations or
stop,
the prohibition or restriction) laying down special conditions on imports, exports and
Veterinary goods transit
l) Regulation of cleansing, restrictions or prohibitions on the use or destruction of the device
and articles that may be carriers of the disease agents
m) Regulation of the special treatment of manure, slurry, manure and waste water,
n) laying down special conditions for storing, collecting, collection, harmless
disposal and other handling of animal by-products,
where appropriate, the regulation of the collection, removal, disposal and other
processing of animal by-products of and outside the specified geographical perimeter
(and modern transporting area),
about editing and hygiene regulation) sanitation service or
technology and work processes, disinfection, disinfestation and
fumigation,
p) restriction or prohibition of the free movement and access of people and their
the collection, restriction or prohibition of frontier traffic of persons,
r) Regulation of disposal, where appropriate, the reduction of sources of animal diseases
with the natural ohniskovostí.
(2) the competent authority shall order emergency health measures
and) when you suspect or confirm the presence of dangerous diseases
or diseases transmitted from animals to humans, or if there is a risk of
its spread (protective and control measures),
(b)) when it detects non-biocompatibility of animal products,
water or feed, or other cause of a serious health threat
animals or animal products, people (health hygiene
measures),
(c)) where there is a danger of the introduction or spread of pathogens of animals and
diseases transmissible from animals to humans or medically harmful
animal products and animal feed from abroad (veterinary measures
the protection of the national territory).
(3) where justified by the circumstances of a particular case may be ordered
other measures appropriate to the animal health requirements and the knowledge
veterinary science.
(4) the competent authority may order emergency health measures also
When you suspect or confirm the presence of other disease or illness
transmitted from animals to humans, which is not considered dangerous (section
17B).
section 55
As the extraordinary health measures on the occurrence of foot-and-mouth
can be ordered by bond, or part of a village. It is understood her
and the access and closure) of access roads to the village, their measures
Gates and warning sign and their guarding,
(b) prohibition of the transit of municipalities and) determine the detours,
(c) establishment of disinfection on) access and access routes into
the village,
d) prohibition on the movement, sale and provision of economic and interest
animals,
(e)) the prohibition of leaving areas in which are placed the sick and suspected
the animals, and the prohibition of entry into these areas without good reason,
(f) a ban on the gathering of persons)
g) laying down rules for the movement of people in the village,
h) prohibition on entry to the village and ban leaving,
I) laying down special conditions for the supply of the municipality, for exceptional
the entry of means of transport and for the entry of people to the village of urgent
the reasons, as well as the determination of the disinfection measures, which must be
means of transport and persons subjected to before leaving the village,
j) determining the special conditions the operation of waste management.
§ 56
A binding opinion
(1) a binding opinion of the State Veterinary Administration, that is not an administrative
the decision is the basis of building management, for the announcement of the construction, and
for the issue of certificate of occupancy, and must be requested
and a professional ^ 10)), in the case of construction or equipment that are subject to
the State veterinary supervision,
(b)) who will be building or use the device as a shelter for animals,
or to store or incineration of animal carcases in the pet food industry.
(2) the authority competent to decide on the matter according to the specific legal
^ 29) legislation can not decide contrary to this opinion.
(3) the Binding references to buildings or facilities that are subject to the State
veterinary supervision and are in buildings that are important for the defense of the State,
shall be issued by the authorities responsible for Defense Minister.
section 56a
(1) Veterinary certificates shall be produced by the official veterinarian on the basis of
made tours (examination) of animals or animal products. Must
is fill in truthfully and completely; must not certify data of which they personally
satisfied and may not sign a certificate which is not filled in, or
only partly filled. Where certain information to certify on the basis of another
document, you must have it before signing the certificates in their possession.
(2) the animal health certificates or other veterinary document, which was
issued by an official veterinarian and has been with animals or animal
products must be
and) on each side shall be signed by the official veterinarian, which is
exhibits, and stamped,
b) drawn up in the official language of the Member State of destination and of the Member
the State in which the border veterinary inspection, or
accompanied by a certified translation into that language (language)
(c) fitted with its own identification number) and it must consist
1. from a single sheet of paper,
2. two or more pages that are part of a single, comprehensive and
sheet of paper, or
3. from several consecutive pages numbered so as to make it clear
on which side of this is the number of sides (for example. "page 2 of 4
party "). The identification number must be indicated on each side,
d) issued before the animals or animal products leave the site
examinations (examinations), and must be accompanied by the original version of the animals, or
animal products upon their entry into the territory of the Member States.
(3) the official veterinarian issuing a health and signs
the certificate may not have such an interest in the animals or certified
animal products, or on the economy, business, or other
the origin of the equipment, in order to have doubts as to its
disinterestedness.
(4) Modify or otherwise abuse the health certificate is issued
disabled.
§ 57
(1) the veterinary authorities shall cooperate with the competent
animal protection authorities, the protection of public health, the State agricultural and
food inspection and professional supervision of feedingstuffs.
(2) the public authorities, the police authorities of the Czech Republic and municipal
the police cooperate with veterinary authorities in the prevention of
dangerous diseases, preventing their dissemination and their control and in
accordance with its terms are involved in ensuring and monitoring compliance with
emergency veterinary measures.
(3) the authorities of the veterinary service are for the performance of State administration in the field of
veterinary care provided
and from the base) a reference population register,
(b)) the data from the agendového information system of population register,
(c)) the data from the agendového information system for foreigners.
(4) the information Provided under paragraph 3 (b). and) are
and) the name or name, last name,
(b)), the date and place of birth; for the data subject, who was born in a foreign country,
the date, place and the State where he was born,
(c)) date and place of death; in the case of the death of the data subject outside the United
Republic, date of death, place and the State on whose territory the death occurred;
If it is issued the Court's decision on the Declaration of death, the date that is in the
decisions listed as the day of death or the date on which the data subject
declared dead have survived, and the date of acquisition of legal power of this
the decision,
(d) the address of the place of stay)
e) nationality, or more of State citizenship.
(5) the information Provided under paragraph 3 (b). (b)) are
and the name or names), surname, maiden name,
(b)), the date and place of birth,
(c) the social security number),
(d) the address of the place of residence),
e) nationality, or more of State citizenship.
(6) the information Provided under paragraph 3 (b). (c)) are
and the name or names), surname, maiden name,
(b)), the date and place of birth,
c) country of citizenship or more of State citizenship,
(d)) the type and address of the place of stay
(e)) the beginning of the stay, where appropriate, the date of their stay.
(7) the data which are kept as reference data in the principal registry
the population recovered from the agendového information system registration
of the population or agendového information system for foreigners only if they are
in the shape of the previous status quo.
(8) of the provided data that can be used in a particular case only
such data, which are necessary for the performance of the task.
TITLE VII
PROFESSIONAL WORK AND ITS PERFORMANCE
§ 58
Professional veterinary activities
(1) the professional veterinary activities
and veterinary preventive activity)
(b)) the investigation, diagnosis and treatment of the animals and surgical
procedures on animals,
(c) prescribing medicines, veterinary) medicines and veterinary
technical resources, medicines and veterinary products,
the sale and dispensing are bound to a veterinarian's prescription,
d) animals for slaughter and meat inspection and investigation of other
animal products,
e) animal health Diagnostics, including veterinary laboratory
Diagnostics,
f) veterinary remediation activities,
g) for more professional activities for which the corresponding qualification
obtained by studying and practice in the health, or even a different scope.
(2) the professional work they perform
and veterinary authorities), in the case of tasks connected with the exercise of State
Administration,
(b)) the State Veterinary institutes and national reference laboratories and
reference laboratories,
c) natural and legal persons to the extent and under the conditions laid down in this
and special legislation, ^ 29a)
(d)) the competent authorities of the Ministry of defence and the Ministry of the Interior.
(3) the professional work may exercise also
and the high school of veterinary) determines if so their status,
(b) secondary vocational school) scope, if this is part of their
pedagogical activities.
§ 59
The competence of the
(1) Persons competent to exercise the professional veterinary activities
are veterinarians, for which it shall be considered as high school graduates,
who have attained the required training during at least five years of full-time
theoretical and practical instruction in the master's degree programme in
the field of veterinary medicine and hygiene ^ 30), involving a study
objects defined by the implementing regulation, a reasonable
knowledge and skills from the courses listed in the implementing
legal provision, which is based on the professional activity of veterinary
doctors.
(2) veterinary surgeons shall also
and) persons holding a diploma, certificate or other evidence of
achieve the desired education, referred to in the implementing regulation
and issued by the competent authority of another Member State,
(b)) persons holding certificates, by which the competent authority of the
the issuing Member State certifies that a diploma, certificate or other
proof of required education
1. in accordance with the requirements referred to in paragraph 1,
2. was obtained so that the person who is the holder of, engaged in
accordance with the law of the relevant activities for the period and under the conditions laid down
for nationals of the Member States in annex 6,
or
3. was issued after their education that is in accordance with paragraph 1, and
It is considered by the issuing Member State as equivalent documents
referred to in point (a)).
(3) persons who are nationals of another Member State and
fulfil the conditions referred to in paragraphs 1 and 2, shall be entitled to use the
they acquired the academic title or Designatory letters, and in a language
the State in which that title has been obtained.
(4) to strengthen the technical competence of official veterinarians
You can use the content of the study, organized by the State Veterinary Administration of the
cooperation with the University with a health curriculum that
occurs in two parts:
and) fundamental (1st grade),
(b)), specialisation (II. degree).
(5) the directors and heads of professional bodies of the State Veterinary
the Administration, as well as State Veterinary institutes, they can exercise only
veterinarians, who have acquired attestation of II. the degree. However, this does not apply
in the case of senior employees in the 1. the degree of control ^ 30a).
(6) the implementing legislation provides for
and that study subjects) must be included in the master's degree
programme in the field of veterinary medicine and hygiene, and fields of study,
of which must be acquired adequate knowledge and skills referred to in
paragraph 1,
(b)), the diplomas, certificates and other evidence of the required education, referred to in
paragraph 2 (a). and)
c) forms, content and organization of the atestačního study of the official health
doctors, method and organization knowledge validation and certification.
(7) if it is not possible to recognize the competence of business
veterinarian in accordance with paragraph 2, or competence for
the performance of the functions of the official veterinarian, shall be done according to the law on
recognition of professional qualifications ^ 31).
§ 59a
the title launched
(1) Persons competent to exercise the professional veterinary activities
scale and in a way corresponding to their professional competence are further
persons who have received
and learning in higher education), master's degree programme in
veterinary medicine or in the field of veterinary hygiene and
Ecology, or studying, which according to a special legal
prescription ^ 31a) considered as equivalent,
(b) studying in higher education) Bachelor's degree program in
the field of veterinary hygiene and ecology, or studying, which according to the
special legal regulation ^ 31a) considered as equivalent,
(c)) the full secondary vocational education or higher professional education in the
the veterinary field,
(d) studying in higher education) degree programme in the area,
that is not listed in subparagraph (a)), or (b)) and that corresponds to the type and
the scope of activities, in particular in the fields of medicine, chemistry or biology,
(e)) the full secondary vocational education or higher professional education in the field,
that is not listed in subparagraph (c)), and that corresponds to the type and extent of
activities,
f) competence for the performance of certain professional veterinary
the activities of the specialized professional preparation
1. an organized State Veterinary Administration, or
2. under special legislation ^ 31b).
(2) persons who have acquired a college education by studying in the Bachelor
study programme in the field of veterinary hygiene and ecology, may
to perform the functions of the official health assistants. Unless otherwise specified in this
the law or the regulations of the European Union, otherwise, the official veterinary assistants
help to the official veterinarian under their guidance and responsibility
in particular, in monitoring compliance with animal health and hygiene conditions
animal husbandry and animal welfare requirements, when you check the marking and
registration of animals and the implementation of the measures set out in the approved
ozdravovacích programmes in monitoring compliance with animal health and
the sanitary conditions and requirements for the handling of animal products,
during the inspection of slaughter animals and meat and in the implementation of the border
veterinary checks.
(3) students of the fourth year of the master's degree and above
programme in the field of veterinary medicine or in the area of animal health
hygiene and ecology are technically eligible for the performance of professional veterinary
the activities carried out within the framework of teaching under the supervision and responsibility of the
veterinarian.
(4) Implementing legislation sets out the Organization, form and scope of the
specialized training for official health assistants.
section 59b
Fitness to practise the profession of veterinary surgeon for persons from third
countries
(1) persons who have acquired competence in third countries, are
to be eligible to exercise the profession of veterinary surgeon, if
a) show that the education received at foreign high
the school is in accordance with the requirements referred to in section 59 paragraph 1. 1 and of this
they will be issued a certificate by the Chamber under a special legal
prescription ^ 32),
(b)) provide proof of certificate of recognition of higher education under the Special
^ law 32a).
(2) a person referred to in paragraph 1, which do not reveal that the education received at the
foreign high school is in accordance with the requirements referred to in section 59 paragraph 1.
1 are eligible to practise the profession of veterinary surgeon on the basis
the successful execution of the differential test ^ 31) of knowledge corresponding to the
requirements referred to in section 59 paragraph 1. 1 (hereinafter referred to as "test").
(3) persons who are applying for the exam, you must provide evidence the certificate
for the recognition of higher education according to a special legal
^ Regulation 32a).
(4) the Examination shall be held prior to the trial, the Chamber shall be established by the Commission as
its advisory body. The members of the examination Board appoints and dismisses the President
On the proposal of the Chamber of the Chamber and veterinary and pharmaceutical
University. Based on tests carried out successfully, the Chamber shall issue
the certificate.
(5) the test can be repeated. The costs associated with making exams
the person referred to in paragraph 3.
(6) on the request of the person referred to in paragraph 3, the Chamber shall refrain from performing
the test, if such a measure is subject to the conditions laid down by law
on the recognition of professional qualifications ^ 31), especially if the person is the holder of
Diploma, certificate or other evidence of the required education. If there was a
from the exam waived, the Commission shall issue a certificate of the fact
within 90 days from the date of submission of the application referred to in the first sentence.
Private veterinarians
section 60
(1) Private veterinarians professionally competent pursuant to § 59 and section 59b
carrying out veterinary therapeutic and preventive activities based on
certificate referred to in the law on Chamber of veterinary surgeons of the Czech
Republic. ^ 32)
(2) when issuing the certificate referred to in paragraph 1 the person professionally
to be eligible under section 59 paragraph 1. 2 may be taken into account on the verified information
of the facts that would be likely to adversely affect the performance of
professional veterinary activities of that person on the territory of the Czech Republic,
provided on a reciprocal basis the Member State from which the person
originates or comes.
§ 61
(1) a private veterinarian is required to
and without delay to the County) to notify the Veterinary Administration of the start and end of the
activities,
(b) inform without delay the regional veterinary) administration of
the occurrence of dangerous diseases, as well as on other relevant facts
the perspective of the veterinary services and the public interest in the performance of its duties,
(c)), when medicines on compliance with withdrawal periods and other
requirements which are laid down in order to avoid undesirable residues
of animal products, or adverse combinations with additional
substances that are contained in animal feed, and to notify the breeder on the
the need for compliance with withdrawal periods for animals that are used for the production of
food,
(d)) lead a proper account of the preventive action taken on the application
and dispensing of medicinal products and of the killing of animals, which are subject to labelling and
register under a special legal regulation ^ 9 d), keep it for a period of
at least 3 years of age and present it on request to the official veterinarian,
e) after its submission shall immediately record in the record keeper
breeder of administration of drugs to animals and the vaccination of animals and completely, correctly and
truthfully fill out the medical certificate.
(2) in the notice of initiation of the activities referred to in paragraph 1 (b). and) must be
listed, in addition to the data provided for the administration of the code of Administration ^ 32b)
academic title, place of veterinary therapeutic and preventive
activities and the telephone number, fax number or e-mail address. To the notification
must be accompanied by the original or a certified copy of the certificate provided for in the law on
Chamber of veterinary surgeons United States ^ 32) and Declaration of consent
with the use of the information provided in the registry and register operations
the information system of the State Veterinary Administration ^ 32 c).
(3) a private veterinarian is obliged to maintain the confidentiality of the
the facts, which they learn about in connection with the performance of professional
veterinary activities, if it has not been absolved. This does not affect
the obligation to notify to the competent authorities certain facts pursuant to this
law and under special legislation. ^ 33)
(4) a private veterinarian is authorized to keep for your records
emergency supply of drugs.
(5) the Examination, health tests and mandatory preventive and diagnostic
within the framework of veterinary checks, checks, health health and inheritance
checks of animal welfare approved for veterinarian performs this
activity. An approved veterinarian progresses in the exercise of this activity
in accordance with the instructions of the regional Veterinary Administration and carries out the activity in the
the scope, procedures and in accordance with the requirements laid down by the Ministry of
According to § 44 para. 1 (b). (d) the veterinarian's Approval) for this
activities of the regional veterinary services may be suspended or
withdrawn, if in its implementation proceeded contrary to the requirements
laid down by this law.
§ 62
(1) a private veterinarian may refuse to provide urgent
professional veterinary help only because of the threat to their health,
which cannot effectively prevent or hinder.
(2) a private veterinarian may withdraw from the contract on the implementation of
professional veterinary Act, if the keeper refused to provide the necessary
synergy. Withdraws a private veterinarian from the Treaty,
provide the animal emergency care, to prevent the suffering of the animal,
damage to his health or other damage, which this care can be
to prevent this.
(3) in the case of urgent action needed in order to prevent, prevent the proliferation of
and control the dangerous disease, or in the interest of ensuring the health
safety of animal products, does not need a private veterinary
physician consent breeders for its implementation.
§ 63
For the content of the request of the private veterinarian about his approval for
the performance of the activities, which require the approval of this Act or the regulations
The European Union, § 61 para. 2 accordingly.
§ 64
Private veterinary technicians
(1) Permission of the veterinary technician to perform some expert
Veterinary operations business generates, by decision of the regional
the veterinary service of the registration of the private veterinary technician.
Permission to private veterinary technician activity also arises
the mere lapse of the time limit and in the manner referred to in section 28 to 30 of the law on freedom of
movement of services. The regional Veterinary Administration decides on the registration, if the
the applicant
and) meets the requirement of professional competence under section 59A(1). 1 (b). (c)),
b) is competent to perform legal acts and upstanding pursuant to § 50 para. 5.
(2) if the applicant is not referred to in paragraph 1 granted identification
number of the person, shall allocate to regional Veterinary Administration identification number
simultaneous with the release of the marketing authorisation referred to in paragraph 1;
the identification number of the person shall provide the registry administrator people ^ 39).
(3) the privacy of veterinary technicians may perform only such separately
professional veterinary acts that correspond to their formal training
eligibility.
(4) otherwise apply to the rights and obligations of private veterinary
technicians reasonably § 61, § 62 para. 1 and 2.
(5) the regional Veterinary Administration may cancel the registration if
private veterinary technician violates the obligations or conditions
arising out of this Act and of the marketing authorisation.
(6) the implementing legislation provides for
and marketing authorisation application) the details referred to in paragraph 1,
(b) the performance of professional veterinary) for details of operations by private
veterinary technology.
§ 64a
The competence for marking livestock
(1) the labelling of animal known as plemenářského law ^ 8) is
a veterinarian or authorized to carry out the private veterinary technician.
(2) the marking of animals known as plemenářského law ^ 8),
including labelling or hot-branded electronic injection
the identifier is further authorized to make the person who has acquired the Central
degree or higher professional education or higher education in the
one of the agricultural sector or in the field with a focus on agriculture,
veterinary and animal health the prevention and from the
specialized professional training with a focus on animal identification
hot-branded, or injection of an electronic identifier passed
final exam and a certificate of eligibility to this
activity.
(3) the marking of animals known as plemenářského law ^ 8), with the
the exception of labelling or hot-branded electronic injection
the identifier is also entitled to make a breeder farm
animals.
(4) Specialized professional training with a focus on animal identification
hot-branded, or injection of an electronic identifier shall organise
high school with a veterinary degree program, issued to persons,
who have undergone this specialist training, a certificate of training
eligibility for marking animals hot-branded or injection
the electronic identifier and maintain a list of such persons.
(5) the implementing legislation lays down the content, scope and organization of the
specialized training focusing on labelling referred to
animals in accordance with the law plemenářského ^ 8) hot-branded or injection
the electronic identifier, method and organization authentication acquired
knowledge, certification and maintenance of a list of persons that
specialized professional training undergone.
TITLE VIII
VETERINARY PREPARATIONS AND VETERINARY TECHNICAL RESOURCES
§ 65
(1) in addition to the scope of the Institute provided for by specific legislation ^ 5)
and) decide, on application by a person established in a Member
States or in one of the parties to the agreement on the European
economic area, for the purpose of putting it into circulation in the United
Republic intends to produce, distribute, from another Member State, or
imported from a third country, veterinary product for approval of veterinary
product and decides on the approval of the changes against the documentation
submitted in the framework of the approval procedure, suspension
decision on the approval of the veterinary medicinal product and the withdrawal of approval
the veterinary medicinal product. To suspend the decision of approval
the veterinary medicinal product or cancel its approval may, if it is established,
veterinary medicine is ineffective is not safe or does not match the
documentation to be submitted in the context of the approval procedure and subsequent amendments,
or if he violates the holder of the approval of the veterinary medicinal product
seriously or repeatedly the obligations established by this Act.
Are not subject to approval, only veterinary medicinal products intended only for export,
(b)), and update the list of authorized veterinary medicinal products,
(c)) at the request of the manufacturer certifies that this producer
in the manufacture of veterinary products complies with the requirements of good manufacturing
practice,
(d)) shall exercise the State veterinary supervision of putting into circulation and use of the
veterinary medicines, monitor compliance with the obligations laid down
This Act, the quality, safety and efficacy of veterinary medicinal products,
e) veterinary products samples taken for laboratory examination,
certifies the quality of veterinary medicinal products, and compliance with the requirements of the
good manufacturing practice,
f) decide on the further use of the veterinary medicinal product in the case of
the findings of its side effects, particularly on the withdrawal of the veterinary
the product from circulation, its destruction, to suspend the application of
the veterinary medicinal product and its marketing and on its entry into
circulation only after the prior consent of the Institute,
g) at the request of the central veterinary administration carries out reviews
specific efficacy of biocidal products against established designers
diseases,
h) assessed in disputed cases, whether it is a veterinary product or
about another product.
(2) the Institute on
and desirability) veterinary technical means and their
safety for animals, monitors their performance and capacity
to achieve the purpose for which they are intended. Leads and updates the list of
Veterinary technical resources
(b)) state veterinary supervision over the usage of veterinary
technical means and monitor compliance with the obligations laid down
This law,
(c)) on the basis of the results of investigation of adverse events related to the
of veterinary technical resources and other knowledge about the
the fact that the veterinary technical means is not suitable for animal health
use, shall decide on the responsibilities
1. to take measures to reduce the adverse effect of the veterinary
technical means, in particular, to suspend its putting into circulation,
to withdraw it from circulation, to terminate its putting into circulation, suspend or
stop using it,
2. remove the defects within a specified period.
(3) the Institute shall examine the completeness of the applications submitted for the approval of the veterinary
the product within 30 days of its delivery. If it finds
incomplete in writing ask the applicant to it within a specified period.
If the request is not within that time made, it can stop the proceedings. The time limit
intended for the completion of the application for approval of a veterinary medicinal product is
not included in the period of 30 days to assess the completeness of the application. On the application for
the approval of the veterinary medicinal product, the Institute shall decide not later than 90 days
the date on which the application is deemed to be complete. If the Department requests and
shall decide on the approval of the veterinary medicinal product, apply this decision after
for 5 years from the date of the decision. The validity of the decision
can be repeatedly extended for another 5 years on the basis of the notifications
the holder of the decision, that it intends to continue to veterinary medicine
produce, distribute, from another Member State or be imported from a third
the land for the purpose of putting into circulation in the Czech Republic; the notification must
be submitted no later than 30 days before its expiration date issued
decision.
(4) in the case of a veterinary medicinal product which has been produced or put into
circulation in the Member State which has its origin in one of the States that
is a Contracting State to the agreement on the European economic area,
the Institute shall be submitted in the request referred to in paragraph 3, only the administrative
the particulars and documents provided for in the implementing legislation. These
the particulars and documents, in particular, showing the conditions under which he was
the country's veterinary product produced or put into circulation
and the period of 90 days shall be reduced to 30 days if
and veterinary medicine) corresponds to the legal regulations, which are for
its production or putting into circulation in that State binding, and
the manufacturing procedures and rules of good manufacturing practice, which are in
the State used and for which there is a sufficiently detailed
documentation, based on which it is possible to carry out additional investigations,
(b)), regulations, procedures and rules referred to under (a)) guarantee
a degree of protection of the legitimate interest that corresponds to the degree of such
protection in the Czech Republic.
(5) the Institute
and in the Gazette) publishes the Ministry of agriculture and in the journal of the Institute of
for State control of veterinary Biologicals and medicaments
1. approval of veterinary medicines and their entry on the list
approved veterinary medicines, including changes, as well as the suspension of the
the validity of the decision on the approval of the veterinary medicinal product, and repealing
its approval,
2. write the veterinary technical resource to the list of technical
resources for veterinary use and cases of adverse events
relating to the use of veterinary technical resources.
Documentation on incidents and their investigation, shall keep for a period of
15 years,
b) stores within their scope of penalties for non-compliance with or breach of
the obligations, requirements or conditions set out in this law.
§ 66
(1) put into circulation and use in the provision of health care is
only possible
a) veterinary medicinal products that have been approved and entered into the List
approved veterinary medicines and have not exceeded the time
their applicability,
(b)) the veterinary technical resources, for which the time is not exceeded
their applicability.
(2) for the scientific, research, teaching and control purposes can also be used
veterinary medicinal products that have not been approved.
(3) in the provision of health care or veterinary
products that are approved in accordance with European Union legislation ^ 34), and
medical devices which are suitable for use within the
veterinary care ^ 34a).
(4) the veterinarian may in the case of threat to life or health
animal use in the provision of health care and such veterinary
technical resource that does not meet the requirements laid down under the
provided that the
and in detail) is with the health of the animal, which was
set accurate diagnosis of his disease. This does not apply only to
Veterinary technical resources that are designed to establish or
confirmation of diagnosis,
(b)) it is not possible to use a different veterinary technical resource that
corresponds to the requirements laid down,
(c)) on the application of the Veterinary Institute became aware of the technical resource that
does not meet the requirements laid down,
(d) met with the breeders) in writing the possible risks of using veterinary
technical resource that does not meet the specified requirements, and breeder
gave voluntary written consent to it.
§ 66a
(1) the decision on approval of the Holders of the veterinary medicinal product is
required to
and) to ensure that the properties of the approved veterinary medicinal product
match the documentation presented in the approval procedure in order to
veterinary medicine were attached instructions for the handling and
ask the Institute for approval of any changes to the content of the data and documentation over
her condition at the time of issue of the decision of approval or approval
the most recent changes, and that before making such changes,
(b) to record and evaluate cases) to report adverse reactions
the authorised veterinary medicinal product, to keep and maintain records about them and
Once a year, is to provide the Institute,
c) in the event of adverse reaction of the approved veterinarian.
of or deficiencies in its make available quality measures to remedy the
and limitations of the adverse effect of the authorised veterinary medicinal product
including its possible withdrawal from circulation, to report within 15 days from the date of
Learn about this Institute the occurrence of serious adverse reaction
the authorised veterinary medicinal product and inform it of
measures,
d) in the event of adverse reaction of the approved veterinarian.
or deficiencies in its product quality to ensure its own cost
examination, or the clinical trial,
(e) introduce the necessary changes), which allow the production, quality control and
the use of the authorised veterinary medicinal product in accordance with the available
scientific knowledge,
(f) the Institute upon request) to provide samples of approved veterinary
of the product and information about the volume of his sales.
(2) the persons that manufacture animal health products are required to
and) produce and control of veterinary medicinal products in a way that will ensure
These products are manufactured and put into circulation in the quality
appropriate to their intended use and in accordance with the particulars and documents
presented by the Institute in the context of the approval of the veterinary medicinal product
or a change in the documentation of the approved veterinary medicinal product, and
to comply with good manufacturing practice,
(b)) to the achievement of the objectives referred to under (a)) of the corresponding system
quality assurance, or hazard analysis and critical
control points (HACCP),
(c)) to take into account in the production of veterinary preparations, the scientific and technical
development,
(d)) are not at the same time the holder of the decision on the approval of the veterinary
of this, inform the holder about all relevant matters
that may have an impact on the quality of the veterinary medicinal product and the responsibility of the
the holder provided for by this Act, and to provide assistance in the
the performance of its obligations under paragraph 1.
(3) persons, which State-approved veterinary products into circulation,
or otherwise treat with them, are required to
and follow the directions to treatment) with the veterinary medicinal product, as referred to
its packaging and the package leaflet,
(b)) be limited to the lowest possible level of adverse impact
the health of humans, animals and the environment,
(c)) report within 15 days from the date on which they were anxious about it, the Institute and the holder of the
decision on the approval of the health of the occurrence of the unwanted
the effect of an approved veterinary medicinal product.
(4) Implementing law provides
and the requirements for an application for approval of) the veterinary medicinal product and the
approval of the amendments to the decision on approval of the veterinary medicinal product,
(b) the requirements for an application) the suspension or cancellation of the
the approval of the veterinary medicinal product,
(c)) the quality requirements of veterinary medicines, as well as substances that
veterinary products must not contain
(d)) details on good manufacturing practice,
(e)) how to report adverse reactions to veterinary medicinal products,
(f) subject to the approval of the changes) to enumerate the resolution changes
of an administrative nature and changes requiring professional evaluation.
§ 66b
(1) the information on the packaging of the veterinary medicinal product must be indicated legibly and
in a meaningful way and in the language of the country in which the veterinary
product is placed into circulation.
(2) if the Institute proceedings for approval of veterinary medicinal product, or
approval of changes to the documentation of the approved veterinary medicinal product,
the proposed designation of the veterinary medicinal product may lead to its
improper use which could result in a danger to
human or animal health or to the environment, within the
of the decision to also provide for the manner in which the mark must be,
or its part, altered, or supplemented.
section 66 c
(1) producers and importers, where applicable, other persons, which State health
technical means into circulation, are required to communicate to the Institute
and) name, surname, residence and identification number of the person, if it is a
a natural person, or the business name, registered office and identification number
the person, in the case of a legal person, number, phone, fax, or
e-mail address,
(b) the start date of the activity) and the place of performance,
(c) information about the permissions) based on which the business is carried on.
(2) manufacturers and importers, who place in the Czech Republic for the first time into circulation
Veterinary technical means shall be required, before it is placed into the
circulation to notify the Institute basic data about this resource. If, on the
by assessing the qualities of this resource Institute finds that it is not
suitable for veterinary use
and) shall inform the manufacturer or the importer,
(b))
1. to end the marketing of that product into circulation, or its
withdrawal from circulation, or
2. the suspension of the marketing of that product into circulation until removal
deficiencies. In this case, it may be the veterinary technical means
again put into circulation only by written consent of the Institute.
(3) the veterinary technical means Resellers are required to
and only those veterinary) selling technical resources
meet the specified requirements, and comply with the conditions for their sale
specified by the manufacturer,
(b)) to ensure that these resources will be provided with instructions, where appropriate, the
further instructions necessary for safe installation, use and maintenance,
including possible disinfection and sterilization, and that these manuals and instructions in
Czech language will be provided to the persons who will
to use,
(c)) and for 5 years to keep documentation on orders, purchase and
the sale of the veterinary technical resources.
(4) persons who used veterinary technical means, and persons
carrying out maintenance and service, are obliged in the case that
confronted with adverse event related to this resource, or the
It learns
and this fact in writing) to notify the Institute. This does not apply if the Department of
on the occurrence of adverse events demonstrably already informed otherwise,
(b) to take without delay the measures imposed).
(5) Implementing law provides
and contains the basic data) that notification of the veterinary technical
the resource specified in the Czech Republic for the first time on the market,
(b)) how and in what time-limits shall be notified to the occurrence of the adverse
events relating to the veterinary technical means used.
TITLE IX OF THE
REIMBURSEMENT OF COSTS AND LOSSES INCURRED IN CONNECTION WITH DANGEROUS DISEASES
§ 67
(1) the Keeper shall pay the costs and losses incurred in the
due to the implementation of the emergency veterinary measures ordered to
control of some of the dangerous diseases and diseases transmissible from animals to
the man, referred to in annex 2 to this Act, and to protect against
their proliferation, or finding the causative agent of the disease or illness, and it
provided that this shall immediately applied measures shall include at least
the isolation of the animals on the holding and the ban on their movement from the time
the emergence of the suspected occurrence of the disease and after confirmation of its occurrence.
(2) the compensation referred to in paragraph 1 includes compensation for
and the costs of culling or) the slaughter of sick
and suspicious animals of susceptible species and destruction of their
carcasses; in justified cases, they also provide a substitute for harmless
the removal of their products,
(b)) or spent the slaughtered animal,
(c)) the cleansing, disinfection, disinfestation, and meanwhile, the economy and its
equipment (equipment)
d) mandated vaccinations,
e) compliance with measures in the protection and surveillance zones, other
the restricted zones,
(f) compliance with the measures laid down in) viewing time before terminating the
emergency veterinary measures and zástavem animals
economy.
(3) in the case of infection or disease transmissible from animals to humans, which
are listed in the regulations of the European Union on expenditure in
the veterinary field ^ 34b), the replacement of
and) for the destruction of contaminated feedingstuffs and contaminated equipment
the economy, which cannot be disinfected in accordance with paragraph 2
(a). (c)),
(b)) for proven losses caused by failure of the production economic
the animal at the time of execution ordered by the emergency veterinary measures
and in connection with them.
(4) in the case of a dangerous disease of bees, also provides compensation for
beekeeping equipment, AIDS, hives and their equipment destroyed or
deactivated based on ordered emergency veterinary measures.
(5) the refund referred to in paragraph 1 shall not be granted if the breeder has not
the obligation to inform the regional Veterinary Administration about suspected presence of
dangerous diseases, or diseases transmitted from animals to humans, other
a major obligation imposed on him by this Act to the prevention,
preventing the spread and control of dangerous infections or diseases communicable
from animals to humans, or mandated to safeguard and control measures.
(6) the Compensation referred to in paragraph 1 shall be reduced by 10%, if
and breeder nezabezpečil transposition laid down) examination, health
of tests and the compulsory preventive and diagnostic operations within the
veterinary checks on health, control of health and control of inheritance
animal welfare, or
b) breeder breeder not fulfilled obligations relating to the labelling and
registration of animals according to plemenářského law ^ 9 d).
§ 68
(1) compensation under section 67 shall be granted in the amount of proven effectively
costs incurred and losses caused.
(2) if it is a replacement for the spent or slaughtered animal, in
the amount of the usual price of a healthy animal of the same species and category in and
the time of the damage, reduced
and) about what was provided for breeders zužitkovatelné parts of the body
animal and zužitkovatelné products
(b)) about 20% of the usual price of the animal, if the animal was euthanized or slaughtered in
as a result of dangerous diseases, if the breeder has not used the possibilities
preventive vaccination, for which a vaccine was approved.
§ 69
(1) persons who ordered the protective and control measures could not
temporarily carry out their usual work or other gainful activity
or it could carry out only to a limited extent, belongs to a substitute for loss of
earnings, if this remedy is not for them from the employer, or
compensation for loss of profit.
(2) persons who have been forced to stay out of that referred to in paragraph
1 outside their place of residence, shall refund the additional cost of temporary
accommodation and catering under special legislation. ^ 35)
(3) the provisions of paragraphs 1 and 2 shall not apply to persons who have been
refund shall be granted under section 67.
section 70
(1) unless otherwise provided in the regulations of the European Union provides the refund
pursuant to section 67 of the State budget, on the basis of the request
the breeder or person referred to in section 69. This request may be made
First, on the first day following the date of culling or slaughter of the animals, and
where there is no culling or slaughter of animals, first day
the following after their ordered protective and control measures, and
within 6 weeks from the date of culling or slaughter of the animals, and
where there is no culling or slaughter of animals, not later than 6 weeks from
the date of completion of the mandated conservation and control measures. If this is
about compensation in case of dangerous diseases of bees, the request may be filed
First, on the first day following the day the killing bees or beehives, and
where there is no killing bees or beehives, the earliest the first day of
following the notification or publication ordered protective and
the disease control measures, and at the latest within 12 weeks from the date of the killing bees
or hives, and where there is no killing bees or beehives, the latest
to 12 weeks from the date of completion of each local ordered the conservation and
measures. To assess whether the conditions for the grant of a refund
and to what extent, will require the opinion of the regional veterinary department
Administration. If the request is not filed in due time, entitlement to the refund shall be lost.
(2) the keeper of a refund may be adequate, according to § 67
backup.
(3) Implementing legislation
and detail) provides for the application of the refund in accordance with § 67 and
requirements for an application is granted, the
(b)) may set on the occurrence of which, in particular, exotic diseases,
where appropriate, the disease transmissible from animals to man the refund
and to what extent.
TITLE X
ADMINISTRATIVE OFFENCES
§ 71
Misdemeanors
(1) a natural person has committed the offence by
and fails to comply with or breach of an obligation) the breeder provided for in § 4, § 5 para.
1 (b). a) to (d)), section 5a paragraph 2. 1, § 6 (1). 1 to 4 and 7, section 7 or section 9
paragraph. 2 and 3,
(b) fails to comply with or breach of an obligation) or security requirements
Health marking of animal products laid down in § 20 para. 4, §
21, art. 1 to 4, 7, 9, 11 and 14, § 25 para. 1, § 27a para. 1, 3 and 4, or
§ 27b para. 1 to 8,
(c) fails to comply with or violate) obligation to protect against diseases and
diseases transmissible from animals to humans in section 11 (1) 1 and 3, § 12 para.
1, § 14 para. 1 or § 16 para. 2, or the obligation of farmers laid down
in § 5 para. 1 (b). e) to (h)) or § 17a. 4,
(d) fails to comply with or violate) the obligation laid down in § 13 para. 4, fails to comply with
or violates any of the measures provided for in § 53 para. 1, or violates the prohibition in §
56A para. 4,
e) fails to comply with or breach of an obligation or security requirements
Health marking of animal products laid down in § 19 para. 1 to
5 or § 20 para. 1 to 3,
(f) fails to comply with or violate veterinary) terms of trade in animals and
animal products or animal health conditions for imports and transit
Veterinary goods from third countries and its exports to these countries,
laid down in § 28 para. 1 to 4, § 29 para. 2, § 30 paragraph 2. 3, § 32 para.
1, 4 and 7, § 34 paragraph 1. 2, § 36 odst. 4, section 38b para. 1 or section 38 c of paragraph 1. 1
up to 4,
g) fails to comply with or breach of an obligation or requirement imposed by a regulation
The European Union on the import of a consignment of products of animal origin for personal
to the Community consumption ^ 21) or the EU regulation on the
animal health requirements applicable to non-commercial movement of pet animals
breeding ^ 48),
(h) violates or fails to comply with) the obligation laid down in § 40 paragraph 2. 1 and section 40 para.
3 and 4 or § 42 para. 3 (b). and)
I) exercises an activity which is subject to authorisation of the Veterinary Administration,
the approval of that body, or registration with that authority, without this
authorisation, the approval or the registration, activity without
the notification or verification of professional competence under the Special
^ 31) law or activity to which it does not appear
eligible,
j) fails to comply with or breach of an obligation or the requirements of the regulations
The European Union in the field of health care, or fails to comply with binding instructions
authority of the veterinary service, or
to fail to comply with or breach of an obligation) resulting for her from exceptional
animal health measures.
(2) a fine may be imposed for the offense to
a) 5 000 CZK in block management,
b) $ 10,000, in the case of an offense referred to in paragraph 1 (b). and) and (b)),
(c)) $ 2,000, in the case of an offense referred to in paragraph 1 (b). c) to (j)),
(d)) of $ 50,000, in the case of an offense referred to in paragraph 1 (b). k).
§ 72
Administrative offences of legal persons and natural persons-entrepreneurs
(1) a legal entity or individual entrepreneur is committed by the administrative
tort by
and fails to comply with or breach of an obligation) the breeder provided for in § 4, § 5 para.
1 (b). a) to (d)) and § 5 para. 2 and 3, section 5a paragraph 2. 1 or § 6 para. 1 to 4
and 7,
(b) fails to comply with or breach of an obligation) or the requirements for the transport of
and care of the animals during transport in section 7 or section 8 paragraph 1. 1, 3 and 4,
c) fails to comply with or breach of an obligation of the promoter Assembly provided for in §
9. 2 and 3, the obligation of the operator to the circus or other public
animal acts provided for in § 9 para. 4 the obligation of the operator
Assembly Centre provided for in § 9a paragraph. 1 and 2 or the obligation to
the trader provided for in § 9b paragraph 1. 1,
d) fails to comply with or breach of an obligation or security requirements
Health marking of animal products laid down in § 20 para. 4, §
21, art. 2, 3 and 11, § 22 para. 1 (b). (d)), § 24 para. 1, § 25 para. 1
up to 4, section 26, section 27 para. 1, § 27a para. 1, 3 and 4 or § 27b para. 1 to 4,
6 and 7,
(e) fails to comply with or violate) obligation to protect against diseases and
diseases transmissible from animals to humans in section 11 (1) 1 and 3, § 12 para.
1, section 14 or section 16 para. 2, or the obligation of the breeder provided for in section 5 of the
paragraph. 1 (b). e) to (h)) or § 17a. 4,
f) fails to comply with or breach of an obligation or security requirements
Health marking of animal products laid down in § 18 para. 1, 2
and 4, § 21, art. 14, § 22 para. 1 (b). a) to (c)) and e) to (j)) or section 23
paragraph. 1 to 3,
g) fails to comply with or violates the obligation provided for in § 39 para. 3 and 4, § 39a
paragraph. 2 and 3, § 40, § 41 para. 1 to 4 or § 42 para. 3 (b). and)
(h) violates or fails to comply with) the obligation laid down in § 13 para. 4, fails to comply with
or violates any of the measures provided for in § 53 para. 1, or violates the prohibition in §
56A para. 4,
I) fails to comply with or breach of an obligation or security requirements
Health marking of animal products laid down in § 19 para. 1 to
5, section 20 (2). 1 to 3 or § 21 para. 1, 4, 7 and 9,
j) fails to comply with or violate the health conditions of trading in animals and
animal products or animal health conditions for imports and transit
Veterinary goods from third countries and its exports to these countries,
laid down in § 28 para. 1 to 4, § 29 para. 2, § 30 paragraph 2. 3, § 32 para.
1, 4 and 7, § 34 paragraph 1. 2, § 36 odst. 4, § 37 para. 3, section 38b para. 1 or
section 38 c of paragraph 1. 1 to 4,
k) fails to comply with or breach of an obligation or requirement imposed by a regulation
The European Union on the import of a consignment of products of animal origin for personal
to the Community consumption ^ 21) or the EU regulation on the
animal health requirements applicable to non-commercial movement of pet animals
breeding ^ 48),
l) exercises an activity which is subject to authorisation of the Veterinary Administration,
the approval of that body, or registration with that authority, without this
authorisation, the approval or the registration, activity without
the notification or verification of professional competence under the Special
^ 31) law or activity to which it does not appear
eligible,
m) fails to comply with or breach of an obligation or the requirements of the regulations
The European Union in the field of health care, or fails to comply with binding instructions
authority of the Veterinary Administration,
n) fails to comply with or breach of an obligation arising for it from the emergency
animal health measures
o) fails to comply with or violates the obligation provided for in § 66a paragraph. 3 or section 66 c
paragraph. 4,
p) fails to comply with or violates the obligation provided for in § 66 para. 4, §66A.
1 and 2, section 66b para. 1 or § 66 c para. 1 to 3, or
q) violates or fails to comply with the obligation laid down in section 66 paragraph 1. 1.
(2) a legal entity or individual entrepreneur is also committed by the administrative
tort by
and) as a private veterinarian who fails to comply with or breach of an obligation
provided for in section 4A(1). 4, § 6 (1). 7, § 12 para. 2, § 17a. 6, §
paragraph 61. 1, 3 and 5 or § 62 para. 2,
(b)) as a private veterinary technician fails to comply with or breach of an obligation
provided for in § 64 para. 3 and 4, or
(c)), as a manufacturer or distributor fails to comply with passports passports or breach
the obligation laid down in section 4b of paragraph 1. 2 or 3.
(3) an administrative offense shall be fined in the
and 300 000 CZK), in the case of an administrative offence referred to in paragraph 1 (b). a) to (d))
and o),
b) 500 000 CZK in the case of an administrative offence referred to in paragraph 1 (b). e) to (g))
and p),
(c) $ 1 0000 0000), in the case of an administrative offence referred to in paragraph 1 (b). (h)) to
m) and (q)),
(d)) $ 2 0000 0000 in the case of an administrative offence referred to in paragraph 1 (b). n),
(e)) $ 50,000, in the case of an administrative offence referred to in paragraph 2 (a). a) to (c)).
§ 72a
cancelled
Common provisions on administrative offences
section 73
(1) a legal person for an administrative offence is not liable if he proves that
made every effort, that it was possible to require that the infringement of the
a legal obligation is prevented.
(2) in determining the amount of the fine to take account of the seriousness of the administrative
offense, in particular, to the manner of its perpetration, duration and its consequences
and the circumstances under which it was committed.
(3) the liability of a legal person for an administrative offense shall cease, if the
the administrative authority has commenced proceedings about him within 2 years from the date on which it
learned, but not later than within 3 years from the date on which it was committed.
(4) The liability for the acts, which took place in the business
person ^ 10) or in direct connection with the applicable provisions of the Act
on the liability of legal persons and sanctions.
§ 74
the title launched
(1) administrative offences under this law in the first instance hearing
the regional Veterinary Administration, to commit the administrative circuit
offence took place, with the exception of administrative offences pursuant to § 72 para. 1 (b). n)
up to p), which dealt with at first instance by the Institute. Offences under section 71
paragraph. 1 (b). (g)) and the administrative offences pursuant to § 72 para. 1 (b). k)
discusses the Customs Office. Violations can be discussed in block management.
(2) the penalty is due within 30 days from the date when the decision on its imposition
came into legal force.
(3) the authority which levied the fine it imposed. Income is income from fines
the State budget.
TITLE XI
PROVISIONS COMMON, TRANSITIONAL AND FINAL
§ 75
(1) compensation for costs and losses incurred by the fulfilment of the obligations under this
the law, in particular the implementation of the imposed emergency veterinary
the measures, the State provides only under conditions and to the extent provided for in this
by law.
(2) If, in the performance of the State veterinary supervision found non-compliance with
or violation of obligations established by this Act, special legal
^ 25 h) regulations or the regulations of the European Union, the State Veterinary
Save management, for which the non-compliance with or breach of the obligation occurred,
full or partial reimbursement of the costs incurred by that authority.
(3) the costs associated with the performance of inspection of slaughter animals and meat and with
Veterinary examination and assessment of the animal products is obliged to
pay the operator of an undertaking, business, or other device in which the
These control activities are carried out, and in the amount of the minimum rates
under the regulations of the European Union governing official controls ^ 35a);
for the purposes of the payment of the amount of costs shall be converted into the Czech currency by
reference exchange rate of the European Central Bank published
By the Commission in the official journal for the relevant period. In the case of tours
bovine animals, which must be in accordance with European Union regulations governing
rules for the prevention, control and eradication of certain transmissible
spongiform encephalopathies ^ 7 c) examined the bovine spongiform
encephalopathy, the refund amount shall be increased by the amount specified by the implementing
legal regulation. Detailed legal regulation also lays down the conditions
investigations, including the age limit of cattle, which must be on the bovine
spongiform encephalopathy has been examined.
(4) if the State Veterinary Administration, that within a specified period not
to correct the deficiencies identified during the routine inspection, the breeder or
the operator of an undertaking, business, or other device in which the
control activities are carried out, shall be obliged to replace the additional costs
checks. The refund of the costs referred to in paragraphs 2 and 3 and the reimbursement of costs for
an additional check by European Union legislation governing official
control ^ 35b) decides the State Veterinary Administration. This compensation is
State budget revenue, it selects the State Veterinary Administration.
The implementing legislation sets out the amount of the lump-sum cost of the additional
checks.
(5) the costs associated with the implementation of the border veterinary control is
obliged to pay the importer or his representative, in the amount of the flat-rate
the amount that corresponds to the actual cost incurred by the implementation of the
border veterinary checks in the previous 2 years. For refund
the costs associated with the implementation of the border veterinary checks shall decide
the regional Veterinary Administration. The replacement is State budget revenue,
It selects the regional animal health management, which it imposed. Detailed
legislation sets out the amount of the lump-sum costs associated with
the implementation of the border veterinary inspection for a period of 2 years.
§ 76
(1) On the procedures under the Act covered by the administrative code ^ 36), if it is not
unless otherwise provided by this Act. The opinion of applied to spatial planning
the documentation is not an administrative decision. Views and opinions issued by the
under this act as a basis for a decision pursuant to the Special
law or territorial approval or notification of construction are
a binding opinion under the administrative code ^ 36a) and are not separate
a decision in the administrative proceedings.
(2) an appeal against a decision of the regional Veterinary Administration pursuant to § 30
paragraph. 2, § 35 para. 1 (b). (b)), § 36 odst. 3, § 42 para. 3 (b). (b)) and §
paragraph 49. 1 (b). (d)) does not have suspensory effect. This decision is
enforceable on the day of the announcement. The decision about changing and termination
emergency veterinary measures pursuant to § 49 paragraph 1. 1 (b). (d)) may be
the first act in the proceedings, unless this cannot be caused by injury to one of the
Parties to the proceedings.
(3) the law on emergency State Veterinary Administration
veterinary measures are referred to the name of the State Veterinary regulation
Administration and
and if a) jurisdiction of the county or any part thereof, in excess of the territorial
the circuit of the village, so that it be posted on the notice board of the regional
the Office and all the municipalities whose territory is concerned, for a period of at least 15
days. The State Veterinary Administration Regulation shall come into force and effect
on the date of its publication; for the day of its publication is considered to be the day of his
posting on the official Board of the regional office. Regulation of the State Veterinary
management must be accessible to everyone in the regional Veterinary Administration,
the regional office and all municipalities whose territory is concerned. This is true
also, mutatis mutandis, for their extraordinary ordered veterinary
measures pursuant to § 17 para. 1, or for the amendment or termination
some of them even before they are completed according to § 17 para. 1,
(b)) to the national nature or relating to territorial districts more counties
kicking off the official boards, ministries and regional authorities, whose
territory is concerned, for a period of at least 15 days and shall be published without delay on
the website of the State Veterinary Administration. If the regulation
The State Veterinary Administration imposed the obligation to others than the
There are breeders of livestock, the State regulation
Veterinary Administration also on a national radio or tv
the broadcast. Regulation of the State Veterinary Administration shall take effect and
effect on the date of its publication; per day shall be the date of its publication in
his posting on the official Board of the Ministry. This applies also, mutatis mutandis, to
their ordered emergency veterinary measures under § 17 para.
1, or for the amendment or termination of some of them before they
the termination pursuant to § 17 para. 1. The operator of a radio or
broadcasters shall allow the representatives of the State free of charge
the veterinary service of the opening of the measures, their modification or
termination as soon as he was asked to do so.
(4) the Administrative Procedure Act does not apply in proceedings
and of the measures referred to in section) of the investigation. 3 and under § 53 para. 1, which
the veterinary inspector shall notify the controlled or required orally to the person
under the inspection procedure; of its findings and ordered measures
record, a copy of which passes a controlled or mandatory.
Controlled person may submit objections against this measure, and that the
the record on this measure, or in writing at the latest within 3 days from the date of
transmission of the record. Lodged objections do not have suspensory effect. The examination of the
objections can completely meet the regional Veterinary Administration; If it fails,
submit the objection without delay to the Central Veterinary Administration, whose
the decision is final, and delivers the controlled person,
(b)) to end the measures pursuant to § 13 para. 5 and under § 53 para. 2; about
termination of these measures shall be drawn up by the regional Veterinary Administration registration
delivers a copy of the controlled person.
section 76a
Unless otherwise provided in this Act,
and) is governed by the recognition of professional competence of the person who is entitled to
such recognition may request and intends to exercise within the territory of the Czech Republic
controlled activity referred to in this law, the law on the recognition of professional
qualification ^ 31),
(b)), the person who is a national of another
the Member State is established and shall be exercised in accordance with its national
regulations of the controlled activity referred to in this Act, to carry out this
activity temporarily or occasionally in the territory of the Czech Republic
the basis of the verification of the documents about her professional competence and written
notification in accordance with the law on the recognition of professional qualifications ^ 31); for this
a person applies, mutatis mutandis, the rights and obligations of the holder of a permit or certificate
under this Act,
(c)) is a trained person, who has obtained a qualification in another Member
State in accordance with the regulations of the European Union and may this qualification
to demonstrate, in a position to carry out the activity on the territory of the Czech Republic in
the scope of these regulations.
§ 77
(1) the proceedings initiated before the date of entry into force of this Act shall be
complete according to the rules active at the time of its launch.
(2) the authorisation for the performance of professional veterinary activities issued pursuant to
the provisions shall be deemed to permit or the registration referred to in
of this Act. If, however, does not permit to operate a rendering
business conditions of this law is the one to whom the authorisation, shall be obliged to
requested within a period of 6 months from the date of entry into force of the law of the State
the Veterinary Administration to decide on the entry permit in compliance with this
by law. If he fails to do so and unless the State Veterinary Administration of the
its own initiative, the previously issued permit expires.
(3) Implementing legislation shall, in accordance with the results of the negotiations
institutions of the European Union and the authorities of the Czech Republic
and) which will be applied during the transitional period
animal health requirements for their operation by way of derogation from the requirements of
laid down in the implementing legislation,
b) divergent animal health requirements for the operation of individual enterprises
referred to under (a)), and the duration of the transitional period.
§ 77a
A binding opinion of the Veterinary Administration, issued as the basis in
construction management, for the announcement of the construction, and for the release of the final building approval
consent, which refers to the buildings and equipment that are destined for breeding
animals to the treatment of animal products and feed or to store,
collection, removal, disposal, and further processing of
animal products, if these activities are carried out
the business way, as well as the buildings that will be used as
shelter for animals pursuant to § 56, shall be issued under this Act, if
their release is replaced by the procedure in proceedings for the issue of an integrated
authorisation in accordance with the law on integrated pollution prevention and control,
integrated pollution registry and on amendments to certain acts (the Act on
integrated prevention). The other provisions of this Act are not
without prejudice to the.
section 77b
The scope of the set by the municipality under this Act are transferred
the scope of the, with the exception of § 46 (a). (c)).
§ 77c
(1) where in the rules of the European Union is talking about
and, the relevant competent authority) to the central authority or competent
the authority shall mean for the purposes of this Act, the Central Office for the
the scope of the performance belongs to permission to do or perform
the relevant measure, or any authority to which it was the performance of the relevant
permissions or implementation of the measures carried over,
(b)) the competent authority or Veterinary Office, this means
for the purposes of this Act, the Veterinary Administration, within whose
the scope of performance of the relevant permissions or were the implementation of the relevant
the measures entrusted to it by this Act, if applicable, within whose jurisdiction the
taking into account its importance, nature and comparable tasks.
(2) the measures to ensure compliance with the obligations to eliminate
the deficiencies and to the consistent application of the requirements under the regulations to
referred to in paragraph 1 shall be carried out in ways set out in this
by law.
(3) persons that are required to fulfil the obligations imposed on them by this
by law, they are required to play in the field of veterinary care responsibilities too,
that for them under the provisions referred to in paragraph 1.
§ 78
Powers of execution
The Ministry will issue a decree to implement section 4A(1). 7, § 4 b paragraph 1. 2 (a).
(d)) and § 4 b paragraph 1. 3 (b). (c)), § 5 para. 4, section 5a paragraph 2. 4, § 6 (1). 8, § 8
paragraph. 5, section 9A(1). 5, § 9b paragraph 1. 3, section 10, paragraph 1. 3, § 17a. 10, § 18
paragraph. 6, § 19 para. 3 and 6, § 21, art. 3, § 21, art. 15, § 21a, para. 5,
§ 22 para. 2, § 23 para. 4, § 24 para. 2, § 25 para. 5, § 27 para. 4, §
27A para. 6, § 27b para. 9, § 28 para. 5, § 31 para. 3, § 33 para. 6, §
34 para. 5, § 37 para. 5, § 38 paragraph 1(a). 4, section 38b para. 3 and 5, section 38 c of paragraph 1.
5, § 39 para. 5, § 40 paragraph 2. 4, § 41 para. 5, § 42 para. 6, § 48 para.
2, § 50 para. 10, § 51a para. 3, § 53 para. 6, § 53a para. 3, § 59
paragraph. 6, section 59A(1). 4, § 64 para. 6, § 64a para. 5, §66A. 4, §
66 c para. 5, § 70 para. 3 and section 75 para. 3-5.
§ 78a
(1) in section 11 (1) 1, § 12 para. 2 (a). (b)) § 13 para. 1 and 2, § 16 para.
2, § 17 para. 2, § 18 para. 2, section 20 (2). 6 and 7 (b). and § 23 paragraph 1). 1
(a). (d)), section 23 paragraph 1. 2, section 27 para. 2 and 3, § 40 paragraph 2. 1 (b). (b)), section 40
paragraph. 5, § 41 para. 1 (b). g) and (h)), § 42 para. 3 (b). a) and b), § 47
paragraph. 4, § 48 para. 1 (b). (d)), § 49 para. 1 and 2, § 50 para. 1, § 51
paragraph. 1, § 64 para. 1 the first and second sentences, § 64 para. 5, § 76 para. 2
and (3) and in the heading to § 49, the words "District veterinary services" in the
the fall and the number replaced by "regional Veterinary Administration" in the
the fall and number.
(2) in section 13(2). 1 (b). (b)) § 16 para. 2, § 40 paragraph 2. 1 (b). and) sentences
the first and second, and (b). (d)) on the first and second place, § 40 paragraph 2. 2 start
the provisions of section a (c). and), § 41 para. 2 and 3, § 54 para. 1 (b). n) on
the first and second place and § 77a, the words "handled animal origin"
in the fall, and the number replaced by "animal by-products"
in the fall, and the number.
PART TWO
cancelled
§ 79
cancelled
PART THREE
cancelled
§ 80
cancelled
PART FOUR
Amendment of the Act No. 368/1992 Coll., on administrative fees, as amended by
amended
§ 81
Act No. 368/1992 Coll., on administrative fees, as amended by Act No.
10/1993 Coll., Act No. 72/1994 Coll., Act No. 85/1994 Coll., Act No.
273/1994 Coll., Act No. 36/1995 Coll., Act No. 118/1995 Coll., Act No.
160/1995 Coll., Act No. 301/1995 Coll., Act No. 151/1997 Coll., Act No.
305/1997 Coll., Act No. 148/1998 Coll., Act No. 157/1998 Coll., Act No.
167/1998 Coll. and Act No. 63/1999 is amended as follows:
The annex to the Act No 368/1992 Coll., on administrative fees, as amended by
Act No. 85/1994 Coll., Act No. 273/1994 Coll., Act No. 36/1995 Coll.
Act No. 118/1995 Coll., Act No. 160/1995 Coll., Act No. 301/1995 Coll.
Act No. 151/1997 Coll. and Act No. 305/1997 Coll., "the scale of the administrative
the fees "shall be amended as follows:
1. item 67:
"The decision about the outcome of the border veterinary checks (section 37
Act No. 167/1999 Coll., on health care and on amendments to certain
related laws)
-for each and any pending ton consignments of live animals-$ 170.0-
-for each and any pending tonne shipment of animal
products, animal feeds and items that can be
carriers of disease agents-$ 110.0-
at least CZK 1 120.0-
a maximum of £ 11 900.0-".
2. item 68, including the note reads as follows:
"and the veterinary medicinal product and Approval)
Veterinary technical
resource (section 65 of Act No. 167/1999 Coll.,
about veterinary care
and amending certain related laws) EUR 3 0.0-
(b)) the issue of certificates for the production of veterinary
preparations and veterinary technical
resources (section 65 of Act No. 167/1999 Coll.,
about veterinary care, and amending
some related laws) EUR 6 0.0-
Note:
The Act referred to in subparagraph zpoplatňovaný, and) this item includes the registration
veterinary medicine and veterinary technical resource
The list of approved veterinary medicines and veterinary technical
resources. ".
3. item 69 reads:
"The issue of a health certificate to transfer the animal out of the bees (§ 6
Act No. 167/1999 Coll., on health care and on amendments to certain
related laws)
-Eur 50.0 per single animal-
-For more than one animal Czk-100.0 ".
4. item 70:
"The issue of the health certificate for the carriage of livestock products
(section 27 of the Act No. 168/1999 Coll. on veterinary care and amending
some related laws) EUR 100.0-".
5. item 71:
"and the issue of certificates of compliance with) the requirements and conditions for the treatment of
the animal products (section 22 of Act No. 166/1999 Coll.
about veterinary care and amending certain
related laws) $ 500.0-
(b) Issue a binding opinion)
(section 56 of the Act No. 168/1999 Coll. on veterinary care
and amending certain related
$ 300.0-laws) ".
6. item 72:
"and private veterinary Registration)
a doctor (section 60 of the Act No. 168/1999 Coll.
about veterinary care, and amending
some related
the laws of) $ 2 0.0-
(b) the Registration of the private veterinary technician) (section 64 of Act No.
166/1999 Coll. on veterinary care and amending certain
related laws)-$ 1 0.0-
(c)) the issue of permits to carry out laboratory, or other
veterinary diagnostic activities (section 50 of the Act No. 168/1999
Coll. on veterinary care and amending
some related laws) EUR 2 0.0-
(d)) issue of permit to operate a rendering of the undertaking (section 50 of the Act
No 166/1999 Coll. on veterinary care and amending certain
related laws) EUR 3 0.0-
(e)) issue of permit to operate other rendering
activities (section 51 of the Act No. 168/1999 Coll. on veterinary care
and amending certain related
laws) CZK 1 0.0-".
7. item 73:
"and the decision of approval) the breeding of dangerous animal species
£ 3 per single animal 0.0-
For more than one animal Eur 5 0.0-
(b) the accreditation of user establishments) to breed animals for
experimental purposes CZK 10-0.0 ".
PART FIVE
REGULATION (EEC)
§ 82
Shall be deleted:
1. Act No. 87/1987 Coll. on veterinary care, as amended by Act No.
239/1991 Coll., Act No. 439/1991 Coll. and Act No. 110/1997 Coll.
2. Law No. 108/1987 Coll., on the scope of veterinary services of the Czech
Republic, as the legal measures of the Bureau of the Czech National Council
No 25/1991 Coll., Act No. 437/1991 Coll., legal measures
Presidium of the Czech National Council No. 348/1992 Coll., Act No. 114/1994
Coll. and Act No. 110/1997 Coll.
PART SIX
The EFFECTIVENESS of the
section 83
This Act shall take effect sixty days after the date of publication.
Klaus r.
Havel, v. r.
Zeman in r.
Annex 1
cancelled
Annex 2
DISEASES AND DISEASES TRANSMISSIBLE FROM ANIMALS TO HUMANS, WHICH ARE CONSIDERED
DANGEROUS, AND THEIR AGENTS
and more common) species:
1. Aujeszky's disease
2. brucellosis (Brucella abortus, Brucella melitensis, Brucella suis)
3. the echinococcosis (hydatidóza)
4. Rift Valley fever
5. hydroperikarditida of ruminants
6. Japanese encephalitis
7. to bluetongue
8. Crimean-Congo haemorrhagic fever
9. leptospirosis
10. listeriosis
11. the cattle plague
12. myiáza (Chrysomya bezziana hominivorax, Cochliomya)
13. paratuberculosis
14. Q fever
15. salmonellosis (invasive serovars-their agents)
16. foot and mouth disease
17. anthrax
18. the transmissible spongiform encephalopathy (TSE)
19. be infested with trichinae
20. tuberculosis (Mycobacterium bovis, Mycobacterium, Mycobacterium suis
Avium, Mycobacterium tuberculosis)
21. Tularaemia
22. or Enterohaemorrhagic Escherichia coli
23. vesicular stomatitis
24. rabies
25. West Nile virus
(b) bovine diseases):
1. bovine anaplasmosis
2. bovine babesiosis
3. enzootic bovine leukosis
4. haemorrhagic septicaemia (pasteurelóza)
5. enough for you
6. IBR (IBR, IBR/IPV)
7. Nodular dermatitis of bovine animals
8. pulmonary disease of cattle
9. theilerióza
10. trichomonáza
11 trypanosomiasis (transmitted by tse-tse fly)
12. bovine genital kampylobakterióza
c) disease of sheep and goats:
1. Enzootic abortion of sheep (sheep chlamydióza)
2. epididymitida Rams (Brucella ovis)
3. the scrapie
4. the plague of small ruminants
5. contagious agalactia
6. infectious pleuropneumonie goats
7. illness Nairobi
8. sheep pox and goat pox
d) disease of horses:
1. equine encephalomyelitis (Eastern)
2. equine encephalomyelitis (Western)
3. dourine
4. infectious anemia horse (equine infectious anaemia)
5. infectious arteritida horses
6. African horse sickness
7. contagious equine metritida
8. piroplasmóza horses
9. Surra (Trypanosoma Evans)
10. Venezuelan equine encephalomyelitis
11. glanders
e) disease of pigs:
1. African swine fever
2. encephalitis caused by Nipah virus
3. classical swine fever
4. swine reproductive and respiratory syndrome
5. swine vesicular disease
6. viral gastroenteritis (transmissible gastroenteritis of pigs)
f) disease of poultry:
1. avian influenza (highly pathogenic and low pathogenic)
2. Pasteurella multocida
3. mykoplasmóza poultry (Mycoplasma gallisepticum, Mycoplasma respiratory)
4. Newcastle disease
5. pulorová disease (Salmonella pullorum)
6. the tyf poultry
g) disease of bees:
1. rot bee brood (European bee fruit rot)
2. Paenibacillus (American bee fruit rot)
3. the Tropilaelaps mite (Tropilaelaps mite infestation of bees)
4. Malawi
5. tumidóza (Aethina tumida)
6. varroáza bees
h) fish diseases:
1. the epizootic haematopoietic necrosis
epizootic ulcerative syndrome 2
3. The Koi Herpes virus (herpes virus of carp Koi)
4. infectious haematopoietic necrosis
5. viral haemorrhagic septicaemia
I) other diseases:
1. the epizootic haemorrhagic disease (deer)
2. leishmaniasis
3. camel pox
j) other diseases for which mandatory reporting decide to institutions of the European
Union.
Annex 3
cancelled
Annex 4
cancelled
Annex 5
cancelled
Annex 6
THE CONDITIONS FOR RECOGNITION OF A CERTIFICATE OF THE COMPETENT AUTHORITY OF THE ISSUING MEMBER
STATE, ATTESTING TO THE LEGAL EXERCISE OF THE PROFESSION OF VETERINARY SURGEON
Germany
In the case of persons whose diplomas, certificates and other evidence of formal
qualifications of veterinary surgeons attest to training
achieved in the territory of the former German Democratic Republic which
does not satisfy all the minimum training requirements provided in § 59
paragraph. 1, the Czech Republic recognises the diplomas, certificates and other documents
of formal qualifications as being sufficient proof if they attest to
training commenced before German unification, they entitle the holder to
the performance of the activities of a veterinary surgeon throughout the territory of Germany under the same
conditions as the documents referred to in section 59 paragraph 1. 2 (a). and) and are complemented by
a certificate issued by the competent German authorities stating that those
persons have effectively and lawfully been engaged in accordance with the activity on the territory of the
Germany for at least three consecutive years during the five
years prior to the date of issue of the certificate.
Estonia
1. in the case of citizens of the Member States whose diplomas, certificates and other
evidence of formal qualifications in veterinary medicine were
granted, or whose training started in, Estonia before the
the accession of the Czech Republic, recognizes the diplomas, certificates and other
evidence of formal qualifications in veterinary medicine as a
sufficient evidence, if they are accompanied by a certificate stating that these
performed effectively and in accordance with the law the activity in
Estonia for at least five consecutive years during the seven
years prior to the date of issue of the certificate.
2. in the case of citizens of the Member States whose diplomas, certificates and other
evidence of formal qualifications in veterinary medicine were
granted, or whose training started in the former Soviet Union
20. in August 1991, the Czech Republic recognises the diplomas, certificates and
other evidence of formal qualifications in veterinary medicine
as being sufficient proof when the authorities of Estonia attest that these documents
have on its territory, the same legal validity as Estonian documents
formal qualifications in veterinary medicine as regards
access to the profession of veterinary surgeon and the exercise of this profession. This
confirmation must be accompanied by a certificate issued by the same authorities
indicating that these citizens of the Member States they have worked effectively and
According to law, the activity on the territory of Estonia for at least five
consecutive years during the seven years prior to the date
issue of the certificate.
Latvia
In the case of citizens of the Member States whose diplomas, certificates and other
evidence of formal qualifications in veterinary medicine were
granted, or whose training started in the former Soviet Union
21. in August 1991, the Czech Republic recognises the diplomas, certificates and
other evidence of formal qualifications in veterinary medicine
as being sufficient proof when the authorities of Latvia attest that these documents
have on its territory, the same legal validity as Latvian documents
formal qualifications in veterinary medicine as regards
access to the profession of veterinary surgeon and the exercise of this profession. This
confirmation must be accompanied by a certificate issued by the same authorities
indicating that these citizens of the Member States they have worked effectively and
According to law, the activity on the territory of Latvia for at least three
consecutive years during the five years preceding the date of issue of
the certificate.
Lithuania
In the case of citizens of the Member States whose diplomas, certificates and other
evidence of formal qualifications in veterinary medicine were
granted, or whose training started in the former Soviet Union
11. in March 1991, the Czech Republic recognises the diplomas, certificates and
other evidence of formal qualifications in veterinary medicine
as being sufficient proof when the authorities of Lithuania attest that those documents have
on its territory, the same legal validity as Lithuanian evidence of formal
qualifications in veterinary medicine as regards access to
the profession of veterinary surgeon and the exercise of this profession. This confirmation
must be accompanied by a certificate issued by the same authorities stating that those
the citizens of the Member States carried out effectively and in compliance with the
activity in the territory of Lithuania for at least three consecutive years in the
during the five years preceding the date of issue of the certificate.
Slovakia
In the case of citizens of the Member States whose diplomas, certificates and other
evidence of formal qualifications in veterinary medicine were
granted, or whose training started in the former Czechoslovakia
1. in January 1993, the Czech Republic recognises the diplomas, certificates and
other evidence of formal qualifications in veterinary medicine
as being sufficient proof when the authorities of Slovakia attest that these documents
have on its territory, the same legal validity as Slovak papers on
formal qualifications in veterinary medicine as regards
access to the profession of veterinary surgeon and the exercise of this profession. This
confirmation must be accompanied by a certificate issued by the same authorities
indicating that these citizens of the Member States they have worked effectively and
According to law, the activity on the territory of Slovakia for at least three
consecutive years during the five years preceding the date of issue of
the certificate.
Slovenia
In the case of citizens of the Member States whose diplomas, certificates and other
evidence of formal qualifications in veterinary medicine were
granted, or whose training started in Yugoslavia before 25.
June 1991, recognized by the Czech Republic the diplomas, certificates and other
evidence of formal qualifications in veterinary medicine as a
sufficient evidence, if the authorities of Slovenia attest that those documents have
on its territory, the same legal validity as Slovenian evidence of formal
qualifications in veterinary medicine as regards access to
the profession of veterinary surgeon and the exercise of this profession. This confirmation
must be accompanied by a certificate issued by the same authorities stating that those
the citizens of the Member States carried out effectively and in compliance with the
activity on the territory of Slovenia for at least three consecutive
years during the five years preceding the date of issue of the certificate.
Bulgaria
In the case of persons whose diplomas, certificates and other evidence of formal
qualifications in veterinary medicine were awarded or whose
the training began in Bulgaria prior to accession, recognized by the United
Republic of the diplomas, certificates and other evidence of formal qualifications
in the field of veterinary medicine as being sufficient proof if they are
accompanied by a certificate stating that such persons have effectively and carry out the
accordance with the law the activity in Bulgaria after for at least three
consecutive years during the five years preceding the date of issue of
the certificate.
Romania
In the case of persons whose diplomas, certificates and other evidence of formal
qualifications in veterinary medicine were awarded or whose
the training began in Romania before accession, acknowledges the United
Republic of the diplomas, certificates and other evidence of formal qualifications
in the field of veterinary medicine as being sufficient proof if they are
accompanied by a certificate stating that such persons have effectively and carry out the
accordance with the law the activity in Romania after for at least three
consecutive years during the five years preceding the date of issue of
the certificate.
The other Member States
In the case of persons from other Member States must be certified by the competent
the Office of the issuing Member State to indicate that this person legal
way participated in the practice of the profession of veterinary surgeon for
at least three consecutive years during the five years
prior to the date of issue of the certificate.
Selected provisions of the novel
Article. (II) Act No. 131/2003 Coll.
PART TWO
TRANSITIONAL PROVISIONS
1. If in other legislation uses the term "District
animal health management ", or" Municipal animal health management in Brno ",
"The municipal veterinary services in Ostrava" and "Municipal animal health management in
Pilsen "shall mean" the regional animal health management ".
2. The District Veterinary Administration, municipal animal health management in Brno,
The municipal veterinary services in Ostrava and the city animal health management in
Pilsen shall cease the effective date of this Act. Their material
property, rights and obligations, including the rights and obligations arising from the
labor relations, that have to date of extinction, moving day
the effective date of this Act to the locally competent regional veterinary
Administration.
3. staff members who are at the date of entry into force of this Act in the
employment relationship to the district health management, urban health
management of technology, Urban veterinary governance in Ostrava and the city
animal health management in Pilsen, become the effective date of this
law staff locally relevant regional Veterinary Administration in
appropriate working, functional and classification.
4. Not permit the performance of professional veterinary activities (50,
51) conditions of this law is the one to whom the authorisation, shall be obliged to
apply within 6 months from the date of entry into force of this Act on the
putting a permit in compliance with this Act. If he fails to do so, and
unless otherwise decided by the competent authority of the Veterinary Administration, on its own initiative,
previously issued permit shall lapse.
5. A natural person who carries on the veterinary preventive, diagnostic
and therapeutic activity business manner based on the decision of the State
the veterinary service of its registration, the effective date of
of this Act, a member of the Chamber and intends to carry out this activity after this
date, shall within 6 months from the date of entry into force of this
the Act to submit a written application for membership of the Chamber and ask for
the certificate referred to in § 60 para. 1 of Act No. 167/1999 Coll., as amended by
of this Act. If he fails to do so, its authorization to pursue those activities
ceases to exist.
6. Farmers and entrepreneurs, ^ 10) who are required to apply for approval
and registration, a registration under this Act, are
required to do so within 6 months from the date of entry into force of this Act.
7. Containers in which they are packaged foodstuffs of animal origin and that
do not bear the health mark may be used
until 31 December 2006. December 2003. Food of animal origin, manufactured before the date of
entry into force of this Act and in storage before that date in State
material reserves, may be put into circulation without the health
mark.
8. In the proceedings that at the date of entry into force of this Act has not been
District veterinary administrations has been finally terminated, continue locally
the regional Veterinary Administration.
9. The provisions of § 35 para. 1 of Act No. 167/1999 Coll., as amended by this
the Act, for the period from the effective date of this Act, the date on which the
entry into force of the Treaty of accession of the Czech Republic to the European
the Union also apply to transiting health item when the output from the
territory of the country.
10. veterinary doctor approved for a particular activity shall be deemed to
date of entry into force of this law all veterinarians to
This day they were registered with the State Veterinary Administration as private
Veterinarians under the former regulations.
10) § 2 (2). 1 and 2 of the commercial code.
Article. (II) Act No. 48/2006 Sb.
Common and transitional provisions
1. the residence permit does not match the performance of professional activities or
approval or registration issued under the existing legislation,
conditions laid down in the regulations of the European communities ^ 38) is the one who
authorisation, approval or registration, shall apply within
6 months from the date of entry into force of this Act on the entry permit,
approval or registration in accordance with these regulations. If he fails to do so
and unless the competent authority of the Veterinary Administration, on its own initiative,
It shall be deemed that permission, approval or registration issued pursuant to the
the existing rules are no longer present.
2. veterinary medicinal products authorised before the date of entry into force of this
the law, which are no longer the veterinary medicinal products in accordance with § 3 (1). 1
(a). t) Act No. 167/1999 Coll., on health care and on amendments to certain
related laws (health law), in the version in force from the date of
entry into force of this law, shall be construed as veterinary products
approved by Act No. 167/1999 Coll. on veterinary care and amending
certain related laws (health law), in the version in force
from the date of entry into force of this Act, unless the additive
used for animal feed, for a period of 3 years from the date of entry into force of
of this Act.
3. Legal proceedings instituted and pending before the date of entry into force of this
Act shall be completed according to the existing legislation.
4. persons who care for stray and abandoned animals in shelters for
animals can carry out this operation until 31 December 2006. in December 2006, even if the
a certificate conferring the right to exercise the activities referred to in § 42 para. 2
Act No. 167/1999 Coll., on health care and on amendments to certain
related laws (health law), in the version in force from the date of
entry into force of this Act.
5. If the products that fall within the scope of Decree No. 377/2003
Coll. on veterinary checks of imports and transit of products from third
countries, as amended, and the relevant provisions of the European
Community ^ 39) and which were imported before 1. January 2005 and stored
in free zones, free warehouses and approved
customs warehouses or premises of persons supplying the vessel in
international maritime transport (section 37), without being accompanied by a health
certificate corresponding to the relevant regulations of the European communities,
have not left the warehouses where they were stored, until 31 December 2006. December 2005 and
remaining in storage shall be from 1. January 2006 destroyed under the supervision of
the official veterinarian ^ 40). The cost of this measure shall be borne by
the owner of the listed products.
6. in other legislation uses the term "handled
of animal origin "means" animal by-products ".
38) European Parliament and Council Regulation (EC) No 852/2004.
European Parliament and Council Regulation (EC) No 853/2004.
European Parliament and Council Regulation (EC) No 854/2004.
European Parliament and Council Regulation (EC) No 1774/2002.
39) Council decision 79/542/EEC, as amended.
Commission decision 94/984/EC, 97/221/EC, 2000/572/EC, 2000/585/EC,
2000/609/EC, 2003/779/EC and 2004/438/EC, as amended.
40) Commission decision 2005/92/EC of 2 October 1998. February 2005 on animal health
conditions, certification and transitional provisions concerning the introduction
and the period of storage of consignments of certain products of animal origin in
free zones, free warehouses and premises of economic
operators supplying cross border means of sea transport in the
The community.
Commission decision 2005/93/EC of 2 October 1998. February 2005 on transitional
provisions concerning the introduction and storage period for consignments of certain
products of animal origin in customs warehouses in the community.
Article. (II) Act No. 182/2008 Sb.
Transitional provisions
1. keepers, which Act No. 167/1999 Coll., in the version in force from the date of
entry into force of this Act imposes an obligation to submit to the County
the Veterinary Administration to approve the program, are required to the healing well
to do so, if this program has not yet been approved, no later than 6
months from the date of entry into force of this Act.
2. the certificate of professional competence, the official veterinary assistant,
which, according to the existing legislation have received person with full
secondary education and successful passing of specialized vocational
training in the relevant area, remain in force even after the acquisition of the
the effectiveness of this Act.
3. the persons who are required under section 5a of the Act No. 167/1999 Coll., on
the version in force from the date of entry into force of this Act, apply for
approval and registration, the registration of establishments keeping
of aquaculture animals shall be obliged to do so within 6
months from the date of entry into force of this Act.
4. Legal proceedings instituted and pending before the date of entry into force of this
Act shall be completed according to the existing legislation.
Article. XXIV Act No 223/2009 Sb.
Transitional provision
The proceedings initiated before the date of entry into force of this law, and to this
the day the unfinished completes and the rights and obligations related to
assessed according to the existing legislation.
Article. (II) Act No. 308/2011 Sb.
Transitional and final provisions
1. The regional Veterinary Administration and Municipal animal health management in Prague as
separate organizational units of the State the effective date of this Act,
disappear by merging the State Veterinary Administration.
2. Employees who are at the date of entry into force of this Act in the
employment relationship to the regional Veterinary Administration and Urban Health
Administration in Prague become the effective date of this Act,
employees of the State Veterinary Administration. Exercise of the rights and obligations of
labor relations of employees who are at the date of entry into force of
This law in employment to regional Veterinary Administration and
City Veterinary Administration Prague, pass to the State Veterinary
Administration.
3. jurisdiction to manage the property of the United States, including the rights and
other assets that were relevant to farm
the regional Veterinary Administration and Municipal animal health management in Prague,
passes the effective date of this Act, the State Veterinary
Administration.
4. From the regional veterinary administrations and city Veterinary Administration in Prague
moving the effective date of this Act, the State Veterinary
management of all receivables, Payables, as well as the rights and obligations
arising from other legislation.
5. the proceedings initiated before the date of entry into force of this Act and to
This day hedge contingent exposures are completed and the rights and obligations associated with it
According to the Act No. 167/1999 Coll., in the version in force until the date of
entry into force of this Act.
6. in other legislation uses the concept of
and) "the State Veterinary Administration" shall mean the central veterinary
the State Veterinary Administration, management
(b)) "regional Veterinary Administration" shall mean the regional veterinary
the State Veterinary Administration, management
(c)) "veterinary authorities" shall mean the State Veterinary
Administration.
7. the operator of company processes and the circulation of various honey
breeders, is obliged to request the regional Veterinary Administration for approval and
the registration of the company pursuant to section 22 paragraph 1. 1 (b). j) Act No. 167/1999 Coll.,
in the version in force from the date of entry into force of this Act, not later than
6 months from the date of entry into force of this Act.
8. The person who places the raw milk into circulation, is required to include this
working in accordance with the Act No. 167/1999 Coll., in the version in force from the date of
entry into force of this Act, not later than 6 months from the date of acquisition
the effectiveness of this Act.
9. A private veterinarian who is obliged to request the regional veterinary
Administration for approval to carry out the examinations, medical exams, and
the compulsory preventive and diagnostic operations within the framework of the health check
animal health and control of inheritance checks of animal welfare within 6 months
from the date of entry into force of this Act.
10. the administrative procedure concerning the renewal of the approval of the veterinary
products and administrative procedures regarding changes to the decision approving the
veterinary products, which has not been completed before the date of
entry into force of this law shall be completed in accordance with the existing laws,
regulations.
1) Council Directive 64/432/EEC of 26 June 1990. June 1964, on animal health
trade in bovine animals and swine within the community.
Council Directive 97/12/EC of 17 May 1999. March 1997, amending and
updating Directive 64/432/EEC on health problems affecting trade in
bovine animals and swine within the community.
European Parliament and Council Directive 2005/36/EC of 6 May 1999. July
2005 on the recognition of professional qualifications.
Council Directive 82/894/EEC of 21 December 1988 December 1982 on the notification of diseases
animals in the community.
Council Directive 88/407/EEC of 14 June 1993 June 1988 on animal health
the requirements for trade in frozen semen of bovine animals deeply inside
The community and imports.
Council Directive 93/60/EEC of 30 June. June 1993 amending Directive
88/407/EEC concerning animal health requirements for trade in quick-frozen
intra-Community trade in bovine semen imports and that its
the scope extends to fresh bovine semen.
Council Directive 2003/43/EC of 26 July 2000. May 2003 amending
Directive 88/407/EEC laying down animal health requirements for trade in semen
bovine animals within the community and imports.
Council Directive 89/556/EEC of 25 September 1992. September 1989 on animal health conditions
trade in embryos of bovine animals in the community and imports of such embryos from
third countries.
Council Directive 93/52/EEC of 24 June 1993. June 1993 amending Directive
89/556/EEC on animal health problems affecting trade in bovine embryos
The community and imports of embryos from third countries.
Council Directive 89/608/EEC of 21 December 1988 November 1989 on mutual assistance
between the administrative authorities of the Member States and their cooperation with the Commission to
ensure the correct application of veterinary and zootechnical legislation
regulations.
Council Directive 89/662/EEC of 11 December. December 1989 on animal health
checks applicable in intra-Community trade with a view to the completion of the internal
the market.
Council Directive 92/67/EEC of 14 June 1993 July 1992, amending
Directive 89/662/EEC concerning veterinary checks in intra-
The community with a view to the completion of the internal market.
European Parliament and Council Directive 2004/41/EC of 21 June 1999. April 2004,
repealing certain directives concerning food hygiene and
health conditions for the production of certain products of animal
origin intended for human consumption and for their placing on the market and which
the changing of Council Directive 89/662/EEC and 92/118/EEC and Council decision
95/408/EC.
Council Directive 91/496/EEC of 15 October 1968. July 1991, laying down the
principles governing the organisation of veterinary checks of animals imported into the
Community from third countries and amending Directives 89/662/EEC,
90/425/EEC and 90/675/EEC.
Council Directive 90/425/EEC of 26 June 1990. June 1990 concerning veterinary and
zootechnical checks applicable in trade in certain live animals and
products within the community with a view to the completion of the internal market.
Council Directive 92/60/EEC of 30 June. June 1992 amending Directive
90/425/EEC concerning veterinary and zootechnical checks applicable in trade with
certain live animals and products within the community with a view to
the completion of the internal market.
Directive of the European Parliament and of the Council 2002/33/EC of 21 June 1999. October 2002,
amending Council Directive 90/425/EEC and 92/118/EEC as regards the
health requirements for animal by-products.
Council Directive 90/426/EEC of 26 June 1990. June 1990, on animal health
conditions governing the movement of equidae and their import from third countries.
Council Directive 92/36/EEC of 29 October April 1992, amending, if
as for African horse sickness, Directive 90/426/EEC on animal health conditions governing
the movement of equidae and their import from third countries.
Council Directive 2004/68/EC of 26 July 2000. April 2004 laying down
animal health rules for the importation of certain live ungulates in
The community, and for their transit, amending Directive 90/426/EEC and
92/65/EEC and repealing Directive 72/462/EEC.
Council Directive 90/429/EEC of 26 June 1990. June 1990, laying down the
animal health requirements for trade in porcine semen for intra-Community
and imports.
Council Directive 90/539/EEC of 15 October 1968. October 1990, on animal health
conditions for trade in poultry and hatching eggs within the community
and imports from third countries.
Council Directive 93/120/EC of 22 December 2004. December 1993 amending
Council Directive 90/539/EEC on animal health conditions governing trade in
poultry and hatching eggs within the community and imports from
third countries.
Council Directive 1999/90/EC of 15 December 1999. November 1999, amending the
Directive 90/539/EEC on animal health conditions governing trade in poultry and
hatching eggs within the community and imports from third countries.
Council Directive 2006/88/EC of 24 July 2003. October 2006 on animal health
requirements for aquaculture animals and products
aquaculture and on the prevention and control of certain diseases in aquatic animals.
Council Directive 91/68/EEC of 28 June 1999. January 1991 concerning the animal
conditions for trade in ovine and caprine animals within the community.
European Parliament and Council Directive 2001/10/EC of 22 December 2004. may
2001 amending Council Directive 91/68/EEC as regards scrapie.
Council Directive 2003/50/EC of 11 July 2001. June 2003, amending Directive
91/68/EEC as regards the tightening of control measures on movements of ovine and
goats.
Council Directive 92/65/EEC of 13 September 1993. July 1992 laying down animal health
regulations for trade in animals, semen, ova and embryos
The community and the introduction into the community, if not subject to the
special Community veterinary legislation listed in Annex A, section I,
Directive 90/425/EEC.
Council Directive 92/118/EEC of 17 May. December 1992 laying down animal health and
health rules for trade in products of animal origin
The community and the introduction into the community, if not subject to the
specific Community rules referred to in annex a(i) to Directive
89/662/EEC and, as regards pathogens, to Directive 90/425/EEC.
Council Directive 96/90/EC of 17 May 1999. December 1996, amending
Directive 92/118/EEC laying down animal health and public health requirements governing
trade in products of animal origin within the community and imports into the
The community, when not subject to specific Community rules
referred to in annex a(i) to Directive 89/662/EEC and, as regards the
pathogens, to Directive 90/425/EEC.
Council Directive 97/79/EC of 18 June 2003. December 1997 amending
Directive 71/118/EEC, 72/462/EEC, 85/73/EEC, 91/67/EEC, 91/492/EEC,
91/493/EEC, 92/45/EEC and 92/118/EEC as regards veterinary control
products entering the community from third countries.
Directive of the European Parliament and of the Council 2002/33/EC of 21 June 1999. October 2002,
amending Council Directive 90/425/EEC and 92/118/EEC as regards the
health requirements for animal by-products.
European Parliament and Council Directive 2004/41/EC of 21 June 1999. April 2004,
repealing certain directives concerning food hygiene and
health conditions for the production of certain products of animal
origin intended for human consumption and for their placing on the market and which
the changing of Council Directive 89/662/EEC and 92/118/EEC and Council decision
95/408/EC.
Council Directive 92/119/EEC of 17 May. December 1992 establishing
General Community measures for the control of certain animal diseases and
specific measures relating to swine vesicular disease.
Council Directive 96/22/EC of 29 April 2004. April 1996 concerning the prohibition on the use of
certain substances having a hormonal or thyrostatic action and of
beta-agonists in stockfarming, and repealing directives 81/602/EEC,
88/146/EEC and 88/299/EEC.
Directive of the European Parliament and of the Council 2003/74/EC of 22 December 2004. September 2003,
amending Council Directive 96/22/EC concerning the prohibition on the use of certain
substances having a hormonal or thyrostatic action and of beta-agonists in
breeding animals.
Council Directive 96/23/EC of 29 April 2004. April 1996 concerning control measures for
of certain substances and residues thereof in live animals and animal
products and repealing directives 85/358/EEC and 86/469/EEC and decisions
89/187/EEC and 91/664/EEC.
Council Directive 96/93/EC of 17 May 1999. December 1996 on the certification for the
animals and animal products.
Council Directive 97/78/EC of 18 June 2003. December 1997 laying down the
the basic rules for veterinary checks on products from third countries
imported into the community.
European Parliament and Council Directive 2001/82/EC of 6 May 1999. November
2001 on the Community code relating to veterinary medicinal products
preparations.
European Parliament and Council Directive 2004/28/EC of 31 October. March
2004 amending Directive 2001/82/EC on the Community code
relating to veterinary medicinal products.
Council Directive 2002/99/EC of 16 December 2002. December 2002 laying down the
animal health rules governing the production, processing, distribution and introduction
products of animal origin intended for human consumption.
Directive of the European Parliament and of the Council 2003/99/EC of 17 May 1999. November
2003 on the monitoring of zoonoses and zoonotic agents, amending Council decision
90/424/EEC and repealing Council Directive 92/117/EEC.
1A) European Parliament and Council Regulation (EC) No 999/2001 of 22 May 2001.
May 2001 laying down rules for the prevention, control and eradication of
certain transmissible spongiform encephalopathies, as amended.
European Parliament and Council Regulation (EC) No 178/2002 of 28 January 2002. January
2002 laying down the General principles and requirements of food law,
establishing the European food safety authority and laying down procedures in
relating to food safety, as amended.
European Parliament and Council Regulation (EU) no 576/2013 of the 12.
June 2013 on non-commercial movements of pet animals and the
repeal of Regulation (EC) No 998/2003. The Commission implementing Regulation (EU) No.
577/2013 of 28 June. June 2013 on sample identification documents
for non-commercial movements of dogs, cats and ferrets, the copies of the list of the territories and
third countries and the requirements for the format, layout and language
a statement attesting to compliance with certain conditions laid down by the
European Parliament and Council Regulation (EU) no 576/2013.
Commission Regulation (EC) No 136/2004 of 22 December 2004. January 2004 laying
laying down procedures for veterinary checks on products imported from third
countries at border inspection posts of the community, as amended.
Commission Regulation (EC) No 282/2004 of 18 February 2004. February 2004
introducing a document for the customs declaration for animals imported into the community
of third countries and veterinary checks of animals, as
the text of the.
Commission Regulation (EC) no 599/2004 of 30 March 2004. March 2004 concerning the adoption of
of a harmonised model certificate and inspection report for trade in
animals and products of animal origin within the community.
Commission Regulation (EC) No 206/2009 of 5 May 1999. March 2009 of import of shipments
products of animal origin for personal consumption in the community and on the
amending Regulation (EC) No 136/2004.
European Parliament and Council Regulation (EC) No 852/2004 of 29 April 2004. April
2004 on the hygiene of foodstuffs, as amended.
European Parliament and Council Regulation (EC) No 853/2004 of 29 April 2004. April
2004, laying down specific hygiene rules for food of
of animal origin, as amended.
European Parliament and Council Regulation (EC) No 854/2004 of 29 April 2004. April
2004, laying down specific rules for the organisation of official
controls on products of animal origin intended for human consumption, in
as amended.
European Parliament and Council Regulation (EC) No 882/2004 of 29 April 2004. April
2004 on official controls performed to ensure the verification of compliance with the legal
provisions relating to feed and food law and animal health rules and
animal welfare, as amended.
European Parliament and Council Regulation (EC) no 1069/2009 of 21 October 2003.
October 2009 laying down health rules for animal by-products
origin and derived products not intended for human consumption, and
repeal of Regulation (EC) No 1774/2002 (the regulation for by-products
of animal origin).
1B) for example, Act No. 20/1966 Coll., on the health care of the people, as amended by
amended, Act No. 258/2000 Coll., on the protection of public health
and amending certain related laws, as amended,
Act No. 155/2000 Coll., on the breeding, breeding and registration of economic
animals and amending certain related laws (plemenářský)
as amended, Act No 246/1992 Coll., on the protection of animals
against cruelty, as amended, Act No. 91/1996 Coll., on
feedingstuffs, as amended, Act No 100/2004 Coll., on
the protection of species of wild fauna and flora
by regulating trade therein, and other measures for the protection of these species
and on amendments to certain acts (the Act on trading in endangered species), in
amended by Act No 444/2005 Coll., Act No. 79/1997 Coll., on pharmaceuticals and on
changes and additions to some related laws, as amended
legislation, Act No. 110/1997 Coll. on foodstuffs and tobacco products and
amending and supplementing certain related laws, as amended
legislation, Act No. 634/1992 Coll. on consumer protection, as amended by
amended.
2) for example, European Parliament and Council Regulation (EC) No 999/2001,
European Parliament and Council Regulation (EC) No 998/2003, regulation
The European Parliament and of the Council (EC) No 178/2002, regulation of the European
Parliament and of the Council (EC) No 852/2004 of the European Parliament and
Council Regulation (EC) No 853/2004 of the European Parliament and Council Regulation (EC) No.
854/2004 of the European Parliament and Council Regulation (EC) No 882/2004,
Commission Regulation (EC) no 745/2004 of the European Parliament and of the Council
(EC) No 1774/2002.
3) Act No. 110/1997 Coll.
Act No. 20/1966 Coll., as amended.
3A) for example, regulation of the European Parliament and of the Council (EC) No 852/2004,
European Parliament and Council Regulation (EC) No 853/2004, regulation
The European Parliament and of the Council (EC) No 178/2002.
4) Act No. 91/1996 Coll., as amended.
4A) European Parliament and Council Regulation (EC) No 183/2005 of the
on 12 June 2006. January 2005 laying down requirements for feed hygiene,
European Parliament and Council Regulation (EC) No 178/2002.
5) for example, Act No. 378/2007 Coll., on pharmaceuticals and on changes of some
related laws (law on medicinal products), as amended,
Act No 120/2002 Coll., on conditions for the placing of biocidal products and
active substances on the market and amending certain related laws, in
as amended, Act No. 91/1996 Coll., on feedstuffs, as amended by
amended.
5A) Decree No. 273/2000 Coll., laying down the maximum permitted
residues of veterinary medicinal products and biologically active substances used in the
livestock production in foods and food ingredients, as amended by
amended.
Council Regulation (EEC) No 2377/90 of 26 June 1990. June 1990 laying
down a Community procedure for the establishment of maximum residue limits of
veterinary medicinal products in foodstuffs of animal origin,
as amended.
6) Act No 246/1992 Coll., as amended.
7) Law No 449/2001 Coll., on game management, as amended.
7A) Constitutional Act No. 347/1997 Coll., on creation of higher territorial
bodies and amending Constitutional Act of the Czech National Council.
1/1993 Coll., Constitution of the Czech Republic, as amended by Constitutional Act No.
176/2001 Sb.
7B) Regulation of the European Parliament and of the Council (EC) no 1069/2009.
for example, 7 c) European Parliament and Council Regulation (EC) No 999/2001.
7 d) Commission decision 2005/91/EC of 2 October 1998. February 2005
period after which the anti-rabies vaccination is considered as valid.
7 g) for example, the European Parliament and of the Council Regulation (EU) no 576/2013
European Parliament and Council Regulation (EC) No 999/2001.
8) Act No. 155/2000 Coll., as amended.
9) § 15 of Act No 246/1992 Coll.
9A) Law No 378/2007 Sb.
Act No. 258/2000 Coll., on the protection of public health and amendment to certain
related laws, as amended.
Act No. 356/2003 SB., on chemical substances and chemical preparations and
amending certain laws, as amended.
9B) European Parliament and Council Regulation (EC) no 1069/2009. Article. 8 and
Annex V European Parliament and Council Regulation (EC) No 999/2001.
9 c) Decree No 291/2003 Coll., on the prohibition of feeding of certain substances
animals, whose products are intended for human consumption, and tracking
(monitoring of the) presence of illicit substances, residues and substances
contaminants to which animal products could be harmful to the
the health of humans, animals and their products, as amended by Decree No.
232/2005 Sb.
9 d) section 22 et seq. Act No. 155/2000 Coll., as amended.
10) § 2 (2). 1 and 2 of the commercial code.
11) Act No. 258/2000 Coll., as amended. Government Regulation
No 27/2002 Coll., laying down the method of organising work and working
the procedures that the employer is obliged to arrange at work related
with breeding the animals.
13) section 28 of the Decree No 136/2004 Coll., laying down details
animal identification and record keeping and registration of the economy and people
established breeding law.
13 c) of Council Regulation (EC) No 1/2005 of 22 December 2004. December 2004 on the protection of
animals during transport and related operations and amending directives
64/432/EEC and 93/119/EC and Regulation (EC) No 1255/97.
14) Council Regulation (EC) No 1/2005 of 22 December 2004. December 2004 on the protection of
animals during transport and related operations and amending directives
64/432/EEC and 93/119/EC and Regulation (EC) No 1255/97.
14A) Commission Regulation (EC) No 1739/2005 of 21 June 2005. October 2005
down the animal health requirements for the movement of circus animals between
by the Member States.
for example, 14B) Council decision 90/424/EEC of 26 June 1990. June 1990 on
expenditure in the veterinary field, as last amended.
14 c) for example, § 52 para. 1 of Decree No. 299/2003 Coll., on measures for the
the prevention and control of diseases and diseases transmissible from animals to man,
section 2 (a). d) Decree No. 202/2004 Coll., on measures for the prevention and
control of African swine fever, section 67 of Decree No. 389/2004 Coll., on
measures for the control of foot and mouth disease and its prevention and on
change of Decree No. 299/2003 Coll., on measures for the prevention and
control of diseases and diseases transmissible from animals to humans, as amended by
Decree No. 356/2004 Sb.
for example, 14 d) European Parliament and Council Regulation (EC) No 852/2004,
European Parliament and Council Regulation (EC) No 853/2004, regulation
The European Parliament and of the Council (EC) No 854/2004 of the European
Parliament and of the Council (EC) No 882/2004 of the European Parliament and
Council Regulation (EC) No 178/2002.
14E) for example, Council Regulation (EEC) No 2377/90, Council Regulation (EEC) No.
315/93 of 8 February 1993. February 1993 laying down Community procedures for the
control of contaminants in food, Decree No. 291/2003 Coll.
Decree No. 273/2000 Coll., Decree No. 132/2004 Coll., on microbiological
the requirements of the food, how they control and evaluation, Decree
No 158/2004 Coll., laying down maximum permitted levels of residues
individual types of pesticides in food and food ingredients,
as amended by Decree No 68/2005 Coll., Decree No 307/2004 Coll., which
define the types of contaminants and toxicologically relevant substances and their
the permissible amount in food.
14F) Article. 5 and section I of annex II to the regulation of the European Parliament and of the Council
(EC) No 853/2004.
Article. 5 (3). 2 and chapter III of annex I to the regulation of the European Parliament and of the
Council Regulation (EC) No 854/2004.
14 g), for example, Decree No 382/2003 Coll., on animal health requirements for
trade in animals and animal health conditions for imports from them
third countries, as amended by Decree No. 260/2005 Coll., Decree No. 381/2003
Coll. on the animal health requirements for aquaculture animals
and the products of aquaculture, fishery products and live bivalve molluscs and on animal health
the terms of their imports from third countries, as amended by Decree No. 201/2004
SB.
14 h) for example, Decree No. 299/2003 Coll., as amended by Decree No 356/2004
Coll., Decree No 389/2004 Coll., Decree No 207/2004 Coll.
14i) Decree 381/2003 Coll., as amended by Decree No. 201/2004 Sb.
15) § 2 (b). a) and b) Act No. 110/1997 Coll., as amended
regulations.
15A) Article. 5 to 8 and annexes I to IV to the regulation of the European Parliament and of the Council
(EC) No 854/2004.
for example, law No 16) 449/2001 Coll., Decree No 244/2002 Coll., which
implementing some provisions of Act No 449/2001 Coll., on game management,
in the wording of later regulations.
17) Law No 102/1963 Coll., on fisheries, as amended.
17A) Council Regulation (EEC) No 1907/90 of 26 June 1990. June 1990 on certain
marketing standards for eggs, as last amended.
Commission Regulation (EC) No 2295/2003 of 23 December 2003. December 2003 laying
introduces the implementing rules for the application of Council Regulation (EEC) No 1907/90 on certain
marketing standards for eggs, as last amended.
Decree No. 327/2001 Coll., implementing section 18 (a). a), (d)), g), (h)),
I) and (j)) Act No. 110/1997 Coll. on foodstuffs and tobacco products and
amending and supplementing certain related laws, as amended
the provisions for meat, meat products, fish, other aquatic life and
products, eggs and products thereof, as amended by Decree No 264/2003
SB.
17 c) Annex III to European Parliament and Council Regulation (EC) No.
853/2004.
17ca) Act No. 500/2004 Coll., the administrative code, as amended by law no 413/2005
SB.
17cb) Act No 119/2002 Coll., on firearms and ammunition, and amending
Act No. 155/2000 Coll., on the validation of firearms, ammunition and
pyrotechnical items and on the amendment of Act No 288/1995 Coll., on fire
weapons and ammunition (the Firearms Act), as amended by Act No.
13/1998 Coll. and Act No 368/1992 Coll., on administrative fees, as amended by
amended, and Act No. 455/1991 Coll., on trades
business (Trade Act), as amended, (the Act on
weapons), as amended.
17 d) Annex I to the regulation of the European Parliament and of the Council (EC) No 854/2004.
17E) Article. 2 (2). 1 (b). h) Regulation of the European Parliament and the Council.
854/2004.
17F) section IV of annex III to European Parliament and Council Regulation (EC) No.
853/2004, as amended.
17 g) European Parliament and Council Regulation (EC) No 852/2004.
European Parliament and Council Regulation (EC) No 853/2004.
European Parliament and Council Regulation (EC) No 178/2002.
Annex I, section IV, Chapter VIII of the regulation of the European Parliament and of the Council
(EC) No 854/2004, as amended.
17 h) Article. 6 (1). 2 and 3 and annex II to the regulation of the European Parliament and of the
Council Regulation (EC) No 852/2004.
Article. 4 (4). 1 to 4 of the European Parliament and Council Regulation (EC) No.
853/2004.
Article. 3 European Parliament and Council Regulation (EC) No 854/2004.
17i) § 1 (b). k) Decree No. 147/1998 Coll. on the method of determination
the critical points in production technology, as amended.
17j) Article. 7 to 9 of the European Parliament and Council Regulation (EC) No 852/2004.
17 k) Law No. 22/1997 Coll., on technical requirements for products and on the
amendments to certain laws, as amended.
17 l), for example, annex III to European Parliament and Council Regulation No.
853/2004, the European Parliament and Council Regulation (EC) No 854/2004.
17 m) Annex I, section II, chapter III of the regulation of the European Parliament and of the
No 854/2004.
17N) annex II, chapter I to III of regulation of the European Parliament and of the Council
(EC) No 854/2004.
17o) Article. 13 of the European Parliament and Council Regulation (EC) No 852/2004.
17 p) annex II, chapter IV of the regulation of the European Parliament and of the Council (EC)
No 852/2004.
Article. 10 European Parliament and Council Regulation (EC) No 853/2004.
Article. 17 of the European Parliament and Council Regulation (EC) No 854/2004.
17q) Decree No 382/2003 Coll.
Decree No. 380/2003 Coll., on animal health requirements for trade in
semen, egg cells and embryos and health conditions
their imports from third countries.
Decree No. 381/2003 Coll.
17R) for example, Commission decision 2001/618/EC of 23 December 2003. July 2001 on
the determination of the additional guarantees relating to Aujeszky's disease to trade with
intra-Community trade, by establishing the criteria for the granting of
information on this disease and repealing decisions 93/24/EEC and 93/244/EEC.
17s) for example, § 12, 14, 30 et seq. Decree No 382/2003 Coll.
17t) Commission Regulation (EC) no 599/2004.
17u) for example, Decree No. 379/2003 Coll., on animal health requirements for
trade in animal products, which are not covered by specific
legislation concerning animal health conditions and their import from third
countries.
for example, article 17v). 8 European Parliament and Council Regulation (EC) No.
853/2004.
17w) § 8 para. 1 of Decree No. 372/2003 Coll. on veterinary checks
When dealing with animals.
§ 7 para. 1 of Decree No 373/2003 Coll. on veterinary checks at
trade in animal products.
17 x) Decree No. 377/2003 Coll. on veterinary checks of imports and
the transit of animals from third countries, as amended by Decree No. 259/2005 Sb.
Decree No. 377/2003 Coll. on veterinary checks of imports and transit
products from third countries, as amended by Decree No. 259/2005 Sb.
17y), for example, Commission Regulation (EC) No 282/2004, Commission Regulation (EC)
No 136/2004.
for example, article 17). 1 Commission Regulation (EC) No 282/2004, art. 2 of regulation
Commission Regulation (EC) No 136/2004.
18) Article. 79 et seq. Council Regulation (EC) No 2913/92 of 12 October 1992. October 1992,
establishing the Community customs code.
18A) Act No. 114/1992 Coll., on nature and landscape protection, as amended by
amended.
Act No 100/2004 Coll., as amended by Act No 444/2005 Sb.
18B) Article. 10 European Parliament and Council Regulation (EC) No 852/2004.
Article. 6 European Parliament and Council Regulation (EC) No 853/2004.
Article. 11 to 15 and annex VI to the regulation of the European Parliament and of the Council (EC) No.
854/2004.
Article. 49 European Parliament and Council Regulation (EC) No 882/2004.
19) of section 217 of the Act No. 13/1993 Coll., as amended.
20) § 145 of Act No. 13/1993 Coll., as amended.
21) Commission Regulation (EC) No 206/2009 of 5 May 1999. March 2009 about imports
consignments of products of animal origin for personal consumption into the community
and amending Regulation (EC) No 136/2004.
23) section 49 of Act No. 13/1993 Coll., the Customs Act, as amended
regulations.
23A) § 3 (b). (h)) and i) Act No 246/1992 Coll., as amended
regulations.
24) Act No. 526/1990 Coll., on prices, as amended.
24A) section 29 of Act No. 222/1999 Coll., on ensuring the defence of the Czech Republic.
25) § 102 paragraph. 2 (a). d) Act No. 128/2000 Coll., on municipalities (municipal
the establishment).
for example, § 25B). 3 Decree No. 299/2003 Coll.
25 c) Act No. 365/2000 Coll., on public administration and information systems of the
amendments to certain other laws.
25 d) European Parliament and Council Regulation (EC) No 2006/2004 on
cooperation between national authorities responsible for the enforcement
compliance with the laws on the protection of consumers ' interests (regulation on cooperation
in the area of consumer protection).
Article 25E). 3 (b). b) European Parliament and Council Regulation (EC) No.
2006/2004 on cooperation between national authorities responsible for the
enforcement of consumer protection laws (the regulation on
cooperation in the field of consumer protection).
25f) Article. 3 (b). k) European Parliament and Council Regulation (EC) No.
2006/2004 on cooperation between national authorities responsible for the
enforcement of consumer protection laws (the regulation on
cooperation in the field of consumer protection).
25 g) Act No. 64/1986 Coll., on Czech commercial inspection, as amended by
amended.
25 g) Article. 2 section 6, art. 3 (2). 2, article. 4 (4). 6 regulation of the European
Parliament and of the Council (EC) No 882/2004.
25 h) section 4 c of law No 249/1997 Coll., on agriculture, as amended by Act No.
291/2009 Sb.
25 h) Law No 185/2004 Coll., the customs administration of the Czech Republic, as amended by
amended.
25I CKS) Article. 48 of Commission Regulation (EC) No 796/2004 of 21 April 2004. April 2004,
laying down detailed rules for the application of cross-compliance, modulation and the
the integrated administration and control system provided for in
Council Regulation (EC) No 1782/2003 establishing common rules
for direct support schemes under the common agricultural policy and establishing
establishing certain support schemes for farmers, as amended.
25I CKS) European Parliament and Council Regulation (EC) no 1523/2007 of 11 July.
December 2007 prohibiting the placing on the market, import to
The community and the export of the cat and dog fur and products containing
These skins.
25j) such as Act No 246/1992 Coll., as amended,
Act No. 79/1997 Coll. as amended, Act No. 110/1997
Coll., as amended.
25 l) Act No. 111/2009 Coll., on basic registers
26) for example, Act No. 110/1997 Coll., as amended,
Act No. 258/2000 Coll., as subsequently amended, Act No. 102/2001
Coll., on general product safety and on amendments to certain acts (the Act on
general product safety), as amended, law No.
634/1992 Coll., as amended.
27) Act No. 553/1991 Coll. on State control, as amended
regulations.
28) Act No. 110/1997 Coll., as amended.
29) Act No. 50/1976 Coll., on zoning and the building code
(the building Act), as amended.
29A) Act No. 381/1991 Coll., on the Czech Chamber of veterinary surgeons
of the Republic.
30) § 44 et seq. Act No. 111/1998 Coll., on universities and amending and
supplement other laws (law on higher education), as amended
regulations.
30A) § 124 of Act No. 262/2006 SB., labour code.
31) Law No 18/2004 Coll., on the recognition of professional qualifications and other
eligibility of nationals of the Member States of the European Union and the
amendments to certain laws (law on the recognition of professional qualifications), as amended by
amended.
31A) § 98 para. 1 of Act No. 111/1998 Coll.
31B) for example, § 1, paragraph 1. 2 Government Regulation No. 10/1999 Coll., which
repeals Decree-Law No. 195/1998 Coll., poison, and some other
substances harmful to health, as amended, and
for the purposes of the Criminal Code provides for what is considered poisons, § 41 para.
4 Act No. 356/2003 SB., on chemical substances and chemical preparations
and amending certain laws, section 44b and 58 of Act No. 258/2000 Coll., as amended by
amended.
32) § 2 (2). 2 (a). (c)) Law No 381/1991 Coll., as amended by Act No.
318/2004 Sb.
32a) § 89 to 90 of Act No. 111/1998 Coll., as amended by Act No. 165/2006.
32B) § 37 para. 2 Act No. 500/2004 Coll., the administrative code.
32 c) Decree No 329/2003 Coll., on State veterinary information system
Administration.
33) for example, Act No. 141/1961 Coll., on criminal court proceedings (the criminal
of procedure), as amended.
34) European Parliament and Council Regulation (EC) No 999/2001.
34A) Act No. 123/2000 Coll., on medical devices and on changing the
some related laws, as amended.
Decree-Law No 336/2004 Coll., laying down technical requirements
for medical devices and amending Government Decree No. 251/2003
Coll., amending certain regulations issued by the Government for the implementation of Act No.
22/1997 Coll., on technical requirements for products and amending and supplementing
certain acts, as amended.
34B) Council decision 90/424/EEC, as amended.
35) Act No. 119/1992 Coll., on travel compensation, as amended
regulations.
Article 35A). 27 and annex IV to the regulation of the European Parliament and of the Council (EC) No.
882/2004.
35B) Article. 28 European Parliament and Council Regulation (EC) No 882/2004.
36) Act No. 500/2004 Coll., the administrative code, as amended by law no 413/2005 Sb.
§ 149 paragraph 36A). 1 Act No. 500/2004 Coll.
37) Annex III, section IX, chapter I, regulation of the European Parliament and of the
Council Regulation (EC) No 853/2004.
38) Annex III, section IX, chapter II, part III, item 1 (b). and) Regulation
The European Parliament and of the Council (EC) No 853/2004.
39) Act No. 111/2009 Coll., on basic registers, as amended by Act No.
100/2010 Sb.
40) European Parliament and Council Regulation (EC) No 854/2004.
European Parliament and Council Regulation (EC) No 882/2004.
41) Article. 11 and 12 of the regulation of the European Parliament and of the Council (EC) No 882/2004.
42) Annex I, section III, chapter III, part of the European
Parliament and of the Council (EC) No 854/2004.
43) section 4 of Act No. 255/2012 Sb.
44) § 7, § 8 (a). and) and (c)), § 9, 20 Act No. 255/2012 Sb.
45) section 7, section 8 (a). (c)), section 9 (b). (b)), section 10 (1). 2, section 20 of Act No.
255/2009 Sb.
46), section 7, section 8 (a). and), c), (e)), and (f)), section 9 (b). (b)), section 10 (1). 2 and § 20
Act No. 255/2009 Sb.
for example, 47) European Parliament and Council Regulation (EC) No 178/2002,
European Parliament and Council Regulation (EC) No 852/2004, regulation
The European Parliament and of the Council (EC) No 853/2004 of the European
Parliament and of the Council (EC) No 854/2004 of the European Parliament and
Council Regulation (EC) No 882/2004 of the European Parliament and Council Regulation (EU) No.
1169/2007 of 25 June. October 2011 on the provision of food information to
consumers, for the regulation of the European Parliament and of the Council (EC) No.
1924/2006 and (EC) No 1925/2006 and repealing Commission Directive 87/250/EEC,
Council Directive 90/496/EEC, Commission Directive 1999/10/EC, directive
European Parliament and Council Directive 2000/13/EC, the Commission directives 2002/67/EC and
2008/5/EC and Commission Regulation (EC) no 608/2004.
48) European Parliament and Council Regulation (EU) no 576/2013.
Article 49). 6 (a). d) European Parliament and Council Regulation (EU) No.
576/2013.
50) the implementing Commission Regulation (EU) No 577/2013.
51) section 20 of Act No. 255/2009 Coll., on the control (control code).