About Feed

Original Language Title: o krmivech

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Read the untranslated law here: https://portal.gov.cz/app/zakony/download?idBiblio=44115&nr=91~2F1996~20Sb.&ft=txt

91/1996 Coll.



LAW



of 15 November 2004. March 1996



about feed



Change: 244/2000 Sb.



Change: 147/2002 Sb.



Change: 320/2002 Coll.



Modified: 21/2004 Sb.



Modified: 21/2004 Coll. (part)



Change: 553/2005 Sb.



Change: 444/2005 Sb.



Change: 214/2007 Sb.



Change: 227/2009 Sb.



Change: 281/2009 Sb.



Change: 33/2010 Sb.



Modified: 18/2012 Sb.



Change: 279/Sb.



Parliament has passed the following Act of the United States:



PART THE FIRST



GENERAL PROVISIONS



§ 1



The subject of the edit



(1) this Act incorporates the relevant provisions of the European

Community ^ 1) and following on directly applicable provisions of the European

Community ^ 1a) lays down certain requirements for the manufacture, import,

use, packaging, labelling, transport and placing on the market of feed,

the additives and premixtures ^ 1b) ^ 1 c), as well as the power and scope of the

professional supervision authority ^ 1 d) compliance with the obligations laid down

This Act and the applicable regulations of the European communities directly

(hereinafter referred to as the "regulations of the European communities").



(2) this Act does not apply to feed, additives and premixtures,

that are intended for export and are safe. ^ 1e)



(3) this Act does not apply to veterinary medicinal products and medicinal products. ^ 2)



§ 2



Definition of terms



(1) in this Act, means the



and unwanted substance or substance) product, present on the surface of or in the

products intended for animal feed, which represent a potential

danger to the health of the animals, people or the environment and which can

have an adverse effect on animal production, with the exception of pathogenic

agents,



(b)) a withdrawal period the minimum period which must elapse from the end

feed intake, that contains a particular additive, for which the

This time limit is set, the slaughter of the animal or early production

animal products intended for food of the people, in order to ensure that the

do not contain residues in quantities in excess of the additives

the maximum limits laid down by the law ^ 2a) veterinary and regulations

Of the European communities,



(c)) conditionally applicable food additive or premix

a feed additive or premixture, which does not meet any of the requirements

provided for in this law, the implementing legislation issued by the

its implementation or the regulations of the European communities, and which cannot be

for this reason, for the original purpose, provided that this

feed additive or a premixture is maintained his health

safety,



(d)) znehodnoceným feed additive premix or feed,

additive or premixture, unfit for animal feed,



(e) the determination of biological testing) efficacy and safety of feedingstuffs, or

the additive,



f) supplier of legal or natural person, in possession of a feed

the additive or premixture, manipulates, or placed on the market,



g) distributor of legal or natural person who conveys

placing the feed additive on the market or the premixture, without the

the product was in the possession of.



(2) for the purposes of this Act, hereafter



and cross-contamination)



1. the occurrence of two or more additives, undesirable substances or

the occurrence of prohibited materials, which have mutual contradictory or

the inhibitory effects, adverse or toxic effects,



2. the occurrence of the undesirable substances or of the forbidden material in the feed or

the occurrence of an additive which is not intended for the species and category

animals,



(b)) supervised the official control ^ 2b),



(c)) by the manufacturer the legal or natural person who manufactures or processes

feed additives or premixtures, has is as a supplier in the possession of

before placing them on the market or is marketing lists; the manufacturer shall mean the

also the person responsible for the manufacture of feed, mobile



(d)) the importer of the legal or natural person, who imports feedingstuffs,

additives or premixtures from third countries,



e) Member State of the European Community also States of the European

economic area and the Swiss Confederation (hereinafter referred to as "the Member

State "),



f) third country a country that is a Member State,



g) product intended for animal feed (hereinafter referred to as "the product")

feed materials, premixtures, additives, feedingstuffs and all other

products intended for use in feedingstuffs or for animal feed.



(3) in this Act, if used in connection with the legal relationships

revised regulations of the European communities, whose content and concepts

importance are not defined in this Act, but in the said legislation,

It is for the purposes of this Act, from the definition of these concepts in the above

legislation.



Basic provisions



§ 3



the title launched



(1) the production, placing on the market and use of feed, an operator must

feed business ^ 2 c) (hereinafter referred to as the "operator") comply with the content and

limits of undesirable substances, in order to ensure the wholesomeness of the ^ 2d).

Products for animal feed with the content of the undesirable substance higher than

the maximum limit of their content, the operator must not be mixed for the purposes

dilution of the same or any other products to feed.



(2) the use of the feed marked withdrawal period, the operator must

comply with the withdrawal period; This is without prejudice to the provisions of the Special

the law ^ 3).



(3) For the manufacture of feedingstuffs of additives and premixtures and animal feed

the operator may not use the products to feed containing the adverse

the substance, if they exceed the limits established by the implementing

by-law, or that contain foreign objects which may endanger health

animals or live storage pest, the list of which lays down the detailed

legal prescription.



(4) for the manufacture of the premixtures should not use the operator as carriers of feed and

substances that their physical characteristics do not achieve

the homogeneity and stability of additives in the premixture.



(5) feed the level of radioactive contamination exceeds the set

limits shall not apply to the operator for more production of complete and

supplementary feedingstuffs, feed placed on the market, import or export.



(6) imports of products for feeding, for which it is required by regulations

Of the European communities of 16), the ^ operator is required to notify in advance

The central control and testing Institute of agriculture (hereinafter referred to as

"the Institute").



(7) the Ministry of agriculture (hereinafter referred to as "the Ministry") lays down the

the Decree



and) the list of undesirable substances and products, and the maximum limits of their content

in products for animal feed,



(b)) list of skladištních pests and their images,



(c)) the maximum levels of radioactive contamination of feedingstuffs intended for direct

animal feed,



d) particular nutritional purposes, their main nutritional characteristics,

determine the recommended period of application and the compulsory particulars on the labelling, including

Declaration and use,



e) list, the purpose and method of use of additives and their protective

period, in addition to additives, subject to the directly applicable

regulations of the European communities ^ 3b).



section 3a



cancelled



section 3b



cancelled



PART TWO



the title launched



§ 4



Approval procedure



(1) a natural or legal person may engage in the activities provided for

European Parliament and Council Regulation (EC) No 183/2005 ^ 4) only

approval of the Constitution.



(2) on approval of the operation of the Institute decides on the basis of the request for approval

operation ^ 5) (hereinafter referred to as "request for approval"), filed on a form issued by the

by the Institute. The Institute publishes the form in a way allowing remote

access.



(3) the request for approval has



a) for natural persons, the name or names and surname, date of birth,

where applicable, the trading name, address of the place of residence, or other

address for service, as a rule, at the place of residence on the territory

The United States, or in a place of business, the identification number of the person (hereinafter

"identification number"), if any; for legal persons

trade name or name, address or another address designated for

delivery, where appropriate, the location of the branch on the territory of the United

of the Republic, and the identification number, if assigned,



(b)) for natural persons established in a third country, name and surname, date of

birth and residence of the person responsible in the Czech Republic; for legal

people registered in a third country, the seat of the branch in the Czech Republic

or the name, date of birth and residence of the person responsible in the United

Republic,



(c) the operation, type of address) activities, and its specification,



d) data, which are the subject of protection of patent rights, and the data that

are identified by a trade secret ^ 6).



(4) according to the type of activity referred to in paragraph 1 as part of the Institute's

the request for approval will require these attachments and copies of documents:



and) details of the feed



(b)) the manufacturing process,



c) technological scheme of production equipment with a description and plan

the arrangement of the production site,



(d) proof of the accuracy of the work) of the mixing device, used for the production of

the final products,



e) proof of inspection or calibration of scales and weighing systems used,



f) quality control plan,



g) verification of the homogeneity of the additives in feedingstuffs and premixtures,



h) data on feed imported from a third country,



I) a written statement by the importer that the product comes from the operation of that

fulfils the requirements according to European Parliament and Council Regulation (EC) No.

183/2005 ^ 3 c),




j) proof of patent protection,



to) copy of the certificate of professional competence of the persons responsible in accordance with § 6

paragraph. 2 or the decision on the recognition of professional qualifications pursuant to section 6 (1). 3,



l) business registration document,



m) the Declaration of the Distributor that feed fulfils the conditions of regulation

The European Parliament and of the Council (EC) No 183/2005 ^ 3 c).



(5) the applicant is obliged to pay for the actions made in the approval

management of the administrative fee under a special legal regulation ^ 22) and

the cost of training and test tasks connected with the approval procedures in the

the amount prescribed by special legislation on compensation for costs

training and test operations ^ 23).



(6) the decision on approval of the operation contains in addition to the General requirements

the particulars referred to in paragraph 3 (b). a) to (c)), the approval

identification number of the service, or any other particulars relating to the operation.



(7) the Institute writes to the registry ^ 7) the identification of the approved

the operation referred to in paragraph 5.



(8) Department of the decision approving the operation be suspended, changed or cancelled



and at the written request of the operator), or



(b)) in cases provided for regulation of the European communities ^ 8).



(9) the operator is obliged to form issued by the Institute announce changes

the data referred to in the request for approval within 30 days of the change.



(10) the Ministry shall issue a decree details the contents of annexes to the application

the approval referred to in paragraph 4.



§ 5



Marketing authorisation procedure



(1) the operator shall conduct the activities provided for in regulation

The European Parliament and of the Council (EC) No 183/2005 ^ 9) is required to apply

Institute for registration (hereinafter referred to as "registration request").



(2) on the registration of the operation of the Institute decides on the application for

registration applications submitted by the operator on a form issued by the Institute. Institute of

exposes the form in a way allowing remote access.



(3) the application for registration contains



a) for natural persons, the name or names and surname, date of birth,

where applicable, the trading name, address of the place of residence, or other

address for service, as a rule, at the place of residence on the territory

The United States, or in a place of business, the identification number, if

allocated; with legal entities, business name or the name, registered office,

or another address for service, if appropriate, the location of the

branches on the territory of the Czech Republic, and the identification number,

If it was allocated, the



(b)) for natural persons established in a third country, name and surname, date of

birth and residence of the person responsible in the Czech Republic; for legal

people registered in a third country, the seat of the branch in the Czech Republic

or the name, date of birth and residence of the person responsible in the United

Republic,



(c) the operation, type of address) activities, and its specification,



d) data, which are the subject of protection of patent rights, and the data that

are identified by a trade secret ^ 6).



(4) according to the type of activity referred to in paragraph 1 as part of the Institute's

application for registration of the requests of these attachments, and copies of documents:



and) details of the feed



(b)) the manufacturing process,



c) technological scheme of production equipment with a description and plan

the arrangement of the production site,



(d) proof of the accuracy of the work) of the mixing device, used for the production of

the final products,



e) proof of inspection or calibration of scales and weighing systems used,



f) quality control plan,



g) verification of the homogeneity of the additives in feedingstuffs and premixtures,



h) data on feed imported from a third country,



I) a written statement by the importer that the product comes from the operation of that

fulfils the requirements according to European Parliament and Council Regulation (EC) No.

183/2005 ^ 3 c),



j) statement of the operator, in writing the processed, and adheres to the

procedures of the system of hazard analysis and critical control points,



k) proof of patent protection,



l) business registration document.



(5) the applicant is obliged to pay for the actions carried out in the registration procedure

the administrative fee under a special legal regulation ^ 22).



(6) the decision on registration of the operation contains in addition to the General requirements

the particulars referred to in paragraph 3 (b). a) to (c)), registration number

operation, or any other particulars relating to the operation.



(7) the Institute writes to the registry ^ 7) the identification of the registered

the operation referred to in paragraph 5.



(8) the Institute shall suspend the operation of the marketing authorisation, amend or withdraw the



and at the written request of the operator), or



(b)) in cases provided for regulation of the European communities ^ 8).



(9) the operator is obliged to form issued by the Institute announce changes

the data referred to in the application for registration within 30 days of the change.



(10) the Ministry shall issue a decree details the contents of annexes to the application

for registration referred to in paragraph 4.



§ 6



The competence of the



(1) the professional qualifications for the manufacture, processing, importation and marketing

the market of additives of certain protein feedingstuffs, premixtures of feed with

the use of additives or premixtures (hereinafter referred to as "professional

eligibility ") means a group of professional and practical knowledge

relating to the production of animal feed, additives and premixtures, knowledge

the foundations of nutrition of livestock and feed technology and knowledge

legal instruments relating to the production of animal feed.



(2) the competence shall be demonstrated by a certificate issued by the Department of

persons who meet the following conditions:



and the eligibility of legal capacity),



(b)) the type, level of education and training in the production of animal feed.



(3) a certificate referred to in paragraph 2 may be replaced by a decision on the recognition of

professional qualifications according to the law on the recognition of professional qualifications of ^ 9b).



(4) the type, level and scope of education and length of professional experience provides

Ministry decree.



§ 6a



(1) nationals of Member States may occasionally or temporarily

the placing on the market in the territory of the Czech Republic, of the additive or feedingstuffs

premixes by verifying the professional qualifications under the Special

law ^ 9b) If you are entitled to carry out continuous performance of this

activities in another Member State. To these persons, the provisions of this

the Act apply, mutatis mutandis, with the exception of section 4 and 5.



(2) the nationals of Member States who are in a Member

the State is authorized to carry out continuous operation of the mobile plant feed, are

required to notify the Institute always at least 3 working days before the start of

production on the territory of the Czech Republic instead of and the timetable for production of animal feed.



§ 7



Requirements for operation and the operator



(1) the operator is obliged to ensure that the



and) operation complies with the requirements of legislation of the European

community, this Act and the implementing regulation,



(b)) in the operation of the specified for the manufacture of animal feedingstuffs, additives or premixtures

He was before, during and after its completion the technically

allow safe access for the collection of samples for the purpose of verifying the quality and

health certificate,



c) feed additives or premixtures containing upper tier

undesirable substances or the occurrence of prohibited materials were stored

separately.



(2) the operator, which operates the mobile feed mill, is obliged to

notify the Institute always at least 3 working days before the start of manufacture place

and the timetable for production of animal feed.



(3) the operator ^ 9 d) is obliged to demonstrate that the Constitution writing process

introduced and observes the procedures of the system of hazard analysis and critical

control points.



(4) the operator that owns, holds, or has imported feed,

the additive or premixture of upper levels of undesirable substances and

products, or the occurrence of prohibited materials or radioactive

contamination, is obliged to notify the Institute and proceed

According to the regulation of the European communities ^ 9e).



(5) the operator must ensure that the records kept in accordance with the regulation of European

Community ^ 9f) kept for 3 years.



(6) the Ministry shall issue a decree



and operations and requirements) of the production installations of the individual

activities laid down in regulation of the European communities ^ 4) ^ 9),



(b) the designation of the place and details) details of a plan

the production of feedingstuffs referred to in paragraph 2,



(c) risk control requirements) for primary producers ^ 9 g).



§ 8



cancelled



§ 8a



cancelled



§ 8b



cancelled



§ 9



cancelled



§ 10



Publication of the list of approved and registered plants



(1) the Institute shall publish, in accordance with the European communities ^ 17)

list of approved and registered in a manner enabling operations

remote access.



(2) Institute of authorised and registered in the list of plants enter the details

set out in section 4, paragraph 4. 5 and § 5 para. 5.



(3) the list of approved operations shall conform to the model set out in

Regulation of the European communities ^ 9 h).



Labelling and packaging



§ 11



cancelled



§ 12



cancelled



section 13 of the



cancelled



the title launched



§ 14



Storage



(1) the operator is obliged to store feed, additives and premixtures

in storage or handling, or production areas to

in accordance with the law of the European communities ^ 9 c)

maintaining the quality of their health and ensure their

protection against



a) misuse,



b) rodents and birds,



c) humidity and substances that may depreciate or

create products harmful to animal and human health and life-threatening


environment.



(2) the operator is required to ensure the implementation of disinfection, disinsection, and

rodent control and maintenance of suitable microclimatic conditions and

purity ^ 10) in the inventory.



§ 15



cancelled



PART THREE



PROFESSIONAL SURVEILLANCE AND TESTING



section 16 of the



(1) the Institute performs at his own expense professional supervision ^ 11) in accordance with the

regulations of the European communities ^ 12) compliance with obligations

provided for in this law and the regulations of the European communities in the field of

feed and animal nutrition; in particular supervises, as operators

comply with the conditions laid down in the manufacture, import, transport, storage,

use or placing on the market of feed additives or premixtures.



(2) the Institute keeps records of defects discovered in the performance of professional supervision.



(3) the Institute shall keep samples of animal feed, additives and

premixtures intended for laboratory testing, in addition to the samples subject to the

the destruction, for a period of 6 months from the date of receipt of the sample to the lab.



(4) if the Department that within a specified period not to delete

the deficiencies found during routine inspection, the operator is obliged to

replace the additional checks cost ^ 12a).



(5) the Ministry shall issue a decree costs an additional lump sum

the checks paid by the operator.



(6) on the reimbursement of costs for the additional inspection shall be decided by the Institute. This

replacement is State budget revenue, selects her Institute.



(7) the operator is obliged to reimburse the costs the Institute for analysis

samples of feed additives and premixtures referred to in the implementing

law ^ 23) if their analysis proves that the samples

do not meet the requirements of this Act and other legislation.



section 16a



cancelled



section 16b



Rapid alert system



(1) the Department is the contact point for the rapid alert system, with

for this purpose, handles the contingency operational plans that set

measures in case of finding that the product is safe to feed and

represents a direct or indirect risk to human health, shall determine

powers, responsibilities and methods of relaying information from within the Institute.



(2) the presence of the product to feed, which cannot be as prescribed by the

Of the European communities ^ 3 c) is considered safe, it is obliged to Institute

notify National contact point ^ 12 c).



§ 17



Sampling and laboratory testing



(1) the sampling and laboratory testing of the quality of feed additives

and premixtures, the Institute performs under professional supervision or on request.



(2) the Institute may perform some laboratory tests, grant

credentials to persons who request it, (hereinafter referred to as "operators

laboratories ").



(3) the list of laboratories of the Institute conducting laboratory testing of the quality

feed additives and premixtures in the performance of professional supervision and

a list of the persons authorized to perform laboratory tests, the Institute shall publish in

Journal of the Central control and testing Institute of agricultural.



(4) an application for the granting of credentials must contain



and) name and surname or business name, place of business,

residence and identification number, if it is a physical person, or a name

where applicable, the trading name, registered office and identification number, if the person

legal,



b) data on the equipment of the laboratory,



(c) the education workers) information about the lab,



d) activities for which the range is to be granted credentials.



(5) the Institute shall grant credentials referred to in paragraph 2 no later than 6 months from the

submission of the application, if



and laboratory equipment) corresponds to the anticipated scope and type

activities by which the requests,



(b)) laboratory tests will be carried out by persons at least secondary

education of chemical or biological,



(c) the results of the laboratory tests at) certification test were found to be in

the range of tolerances laid down for these tests.



(6) the Institute has overseen, that the last conditions under which accreditation has been given

in accordance with paragraph 5.



(7) the Institute may change or revoke the credentials if you have changed or

have ceased to apply the conditions under which accreditation has been granted. At the written request

the lab operator, the Institute shall cancel the credentials.



(8) the Institute and the operators are required to ensure the laboratories

objectivity and comparability of the results of the checks follow

requirements for sampling and use methods of laboratory testing, in

accordance with the European communities ^ 13).



(9) the Ministry shall issue a decree



a) requirements for the sampling for the official control of residues

pesticides in products for animal feed,



(b)) the manner of publication of laboratory testing methods and procedures in official

inspection of products for feeding, unless the methods set out in the regulations

Of the European communities ^ 18).



section 18



Special measures



(1) If, in the exercise of professional supervision Institute found that a feed

additive or premixture do not meet the requirements of this Act,

the implementing legislation or regulations of the European communities,

the decision saves the operator measures according to the regulations of the European

Community ^ 13a).



(2) if the Institute its own investigation or on the basis of the communication law

or natural person finds that occurred or is occurring to the fact

that can compromise the safety of the feed additive or premixture,

follow the regulation of the European Parliament and of the Council (EC) No 178/2002

and the regulation of the European Parliament and of the Council (EC) No 882/2004 ^ 13b).



(3) in the case of conditionally applicable animal feed, additives or premixtures

the Institute provides for special measures in the decision to use the replacement

and shall determine the conditions of use.



(4) an appeal against a decision on the measures referred to in paragraphs 2 and 3

does not have suspensory effect.



(5) the operator must within the time limit laid down specific measures

inform the Institute about how to meet their obligations.



§ 19



cancelled



§ 19a



Administrative offences of legal persons and natural persons-entrepreneurs



(1) a legal entity or individual entrepreneur is committed by the administrative

tort by performing activities in accordance with § 4 para. 1 without the consent of

of the Institute.



(2) a legal entity or individual entrepreneur as an operator

committing an administrative offense, by



and produces, uses,) bring or launches a feed additive

or premixtures in violation of § 3 para. 1 to 6,



(b) fails to notify the Institute changes) information referred to in the request for approval under section

4 (4). 8,



(c)) carries out activities pursuant to § 5 para. 1 without registration service or

fails to notify changes to the data referred to in the application for marketing authorization pursuant to § 5 para.

8,



(d)) does not ensure any of the requirements of the operation in accordance with § 7 paragraph 1. 1 (b). and)

or (b)),



(e)) does not provide separate storage of feedingstuffs, additives or premixtures

pursuant to § 7 para. 1 (b). (c)),



f) operates mobile mill feed and does not notify the location or time schedule

the production of feedingstuffs pursuant to § 7 para. 2,



g) does not process does in writing or does not comply with the procedures pursuant to § 7 para.

3,



(h)) does not notice or does not flow under § 7 para. 4,



I) does not retain records pursuant to § 7 para. 5,



j) fails to comply with an obligation imposed special measures under section 18,



k) produces or presents on the market of raw materials or products that have been

acquired or modified using new technological processes or that

do not yet have the character of a feed, without the permission of their production or marketing

on the market under section 21a, para. 2,



l) contrary to the directly applicable European Community law

governing the use of the feed and their placing on the market of ^ 19) applies or

on the market of feed additives or premixtures which are not

safe or have a direct negative effect on the environment or

animal welfare,



m) does not ensure the designation, presentation or packaging of feed additives

substances or pre-mixes in accordance with regulations of the European communities,



n) neuskladní feed additives or premixtures according to § 14 para. 1

or does not ensure the implementation of disinfection, disinsection or rodent control pursuant to §

14. 2,



about) does not ensure the transport of feedingstuffs, premixtures of additives or in accordance with the

regulations of the European communities,



p) does not accept the corresponding sanitary measures provided for directly

the applicable law of the European communities ^ 9 c),



q) contrary to the directly applicable European Community law

governing the requirements for feed hygiene removes or applies a feed

additives or premixtures of unregistered or unsanctioned

operations ^ 20), or



r) violates any other obligation specified in the provisions of the European communities in

feed ^ 1a).



(3) the operator of a laboratory is guilty of an administrative offense to the fact that

contrary to section 17 para. 8 does not flow according to the requirements for the subscription

samples or apply methods laid down for the procedure in the laboratory

testing.



(4) an administrative offense shall be fined in the



and 750 000 CZK), in the case of an administrative offence referred to in paragraph 2 (a). I) to (l)),



b) 500 000 CZK in the case of an administrative offence referred to in paragraph 1, paragraph 2

(a). a), d), (e)), g), (h)), m) to q) or in accordance with paragraph 3,



c) 250 000 CZK in the case of an administrative offence referred to in paragraph 2 (a). (b)), (c)),

(f)) or r).



§ 19b



cancelled



§ 19 c



Provisions common to administrative offences



(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 on a legal person shall take account of the seriousness of the

the administrative offense, in particular, the way a criminal offence 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

administrative authority about him has not initiated proceedings within 1 year 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 or in direct connection with him, subject to the provisions of the law on

liability and sanctions legal persons.



(5) administrative offences under this law in the first instance hearing

Institute.



(6) the Fines collected by the Institute. Income from fines is the State budget revenue.



PART FOUR



PRODUCTION AND IMPORT OF FEED FOR RESEARCH PURPOSES



section 20



(1) the production and importation of the experimental compound feedingstuffs and premixtures for experimental

biological testing necessary for the implementation of a scientific or

the research plan, unless they comply with the conditions laid down in this

Act or the regulations of the European communities ^ 21) may only be performed by

Institute, manufacturers and importers of approval or registered under section 4 or 5

This law, which the Ministry grants for this production and imports

the authorization. This provision shall not apply to feed for toxicological

tests and experimental compound feedingstuffs manufactured and used in the facilities of universities and

Scientific and research institutions.



(2) an application for authorization must contain



a) name and address of the natural person or business name and address of the legal

the person responsible for carrying out scientific or research project,



(b) the name and address of the approved) or a registered manufacturer who will

the production of experimental compound feedingstuffs and premixtures and the seat of the establishment,



(c) the designation of the feed, tested) feed materials, additives or

pre-mix,



(d)) the nutrient content and level of the additives, if present,



e) for feed materials and additives, the method of production,



(f)) in the test compound feedingstuffs or pre-mixtures experimental composition,



(g)) the production volume,



(h) other information indicating the feed), feed materials, additives or

premixtures.



(3) the applicant shall attach to the request, the consent of the State Veterinary Administration ^ 2a)

or the competent authority of the environmental inspection, saying that the test

feed, feed material, additive or premixture in the proposed

the use does not threaten the health of humans, animals and the environment.



section 21



(1) the Ministry shall grant an authorisation, provided that the manufacturer shall ensure



and the contamination of the device) and the rest of the traffic

test feed, feed ingredient, premix or feed additive or

produced by the experimental feed,



(b)) the separate storage of the test feed, feed materials, additives

the substance of the premixture and produced experimental compound feedingstuffs,



(c) a separate record of the production of experimental) compound feedingstuffs and premixtures, and

the purpose of the test used in feed, feed materials,

substances or premixtures



(d) the indication of the test), feed materials, feed additives

substances, premixtures and produced experimental mixtures or "designed for pre-mix

experimental purposes ... ", including the name and quantity of the contained test

substance in 1 kg.



(2) the Ministry shall revoke the authorisation for the production of experimental mixtures and premixtures

If there is a breach of the conditions under which authorisation was granted, or

the written request of the manufacturer.



§ 21a



Biological testing



(1) a natural or legal person who proposes to produce, or be placed on the

the market feed materials or products obtained or modified

by using new technological processes or which do not yet have the character

feed, must submit to the institution of the positive result of the summary dossier

biological testing conducted according to the procedures and conditions laid down

an implementing regulation. The Institute may require other necessary

special expertise.



(2) the Institute shall issue a permit for the manufacture or placing on the market of the feed material

or a product that has been produced or modified by the new

technological processes or who did not yet have the character of feed, for

provided that the procedures and conditions have been fulfilled in accordance with paragraph 1.



(3) the biological testing referred to in paragraph 1 shall carry out the Institute or legal

or natural persons to whom the Institute shall grant to perform biological testing

credentials. The cost for biological testing shall be borne by the person testing

requested and that is required to deliver the required amount of free of charge

raw material or product to test.



(4) an application for the granting of credentials to perform biological testing must

contain



a) for natural persons, the name or names and surname, date of birth,

where applicable, the trading name, address of residence, otherwise the address

for service, usually in the place of residence on the territory of the United

the Republic or at the place of business, the identification number, if

allocated; with legal entities, business name or the name, registered office,

where appropriate, the location of the branch on the territory of the Czech Republic, and

the identification number, if assigned,



(b)) for natural persons established in a third country, name and surname, date of

birth and residence of the person responsible in the Czech Republic; for legal

people registered in a third country, the seat of the branch in the Czech Republic

or the name, date of birth and residence of the person responsible in the United

Republic,



(c) data on-the-spot implementation) biological testing, scope and type

testing, animal hygiene parameters and technological equipment,



(d) details of education workers) who will perform a biological

testing,



(e)) the range of activities, the nature and category of animals on which the biological

testing is carried out.



(5) the Institute shall grant credentials to perform biological testing by

within 6 months from submission of the application, if



and) Zoo-hygienic parameters and technological facilities correspond to the

the anticipated scope and type testing,



(b)) the person responsible for the implementation of biological testing has at least

complete secondary education natural history focus,



(c)) will be allowed to carry out an inspection of the place of Institute personnel performing

biological testing and assessment of suitability for the desired

the scope and intent of the biological testing.



(6) the Institute has overseen, that the last conditions under which accreditation has been given

in accordance with paragraph 5. The Institute may change if the credentials have changed

the conditions under which accreditation has been granted. The Department may revoke the credentials

If these conditions have changed significantly, or have passed away. On the basis of

a written request from the operator, the Institute shall cancel the credentials.



(7) the biological testing conducted on the animal experiment shall be

carried out under the conditions laid down by the law on the protection of animals against

cruelty ^ 13d).



(8) Testing the effectiveness and safety of new additives or

their new use, including additives intended for the manufacture of

feed, process documentation and monographs is performed according to the procedures

under the regulations of the European communities ^ 13e).



(9) the Ministry shall issue a decree



and the summary dossier) the details of biological testing,



(b)) and the methods for implementing the technical parameters of biological testing of feed,

including the methods of testing the effectiveness of additives intended for the

the manufacture of feedingstuffs and the methods of testing the quality of animal products.



PART FIVE



section 22



cancelled



Article 23 of the



Transitional provision



Registration of producers and importers under the previous legislation, ^ 14)

does not lose validity, if within one year from the entry into force of the Act

the manufacturer or importer requests registration pursuant to section 8 of this Act, and

If at this time meet the requirements referred to in articles 6 and 7 of this Act. In this

the case is not subject to the registration administrative fee.



section 24



Regulation (EEC)



Are deleted;



and section 31 (a)). f) and (g)), and in section 32 (a). e) part of the sentence "the quality authentication

feed, feed mixtures and raw materials used to manufacture them, as well as "

Act No. 61/1964 Coll., on the development of plant production,



(b) the Decree of the Ministry of agriculture) of the Czech Republic No. 413/1991 Coll., on the

the registration of certain types of feed, their suppliers and professional State

check



(c) the Decree of the Ministry of agriculture) of the Czech Republic No. 362/1992 Coll., on the

production and composition of compound feedingstuffs, as amended by decrees no. 258/1993 Coll. and no.

190/1995 Sb.



§ 25



The effectiveness of the



This Act shall take effect on 1 January 2000. September 1996.



Uhde in r.



Havel, v. r.



Klaus r.



Selected provisions of the novel



Article II of Act No. 247/2000 Coll.



Transitional provisions



1. Registration of producers and importers, made before the effective date of this Act,

does not lose validity if within 18 months from the entry into force of this

the law, the manufacturer or importer shall request registration under section 8 and, if

This time will meet the requirements under sections 4 to 7. In this case, is not subject to

registration administrative fee.



2. suppliers and distributors, covered by the obligation to register

pursuant to section 8 and 8a are required to apply for registration within 3 months from the date of

entry into force of this Act.



3. products in packages marked in accordance with the existing legislation


may be put into circulation, but within 6 months from the date of acquisition

the effectiveness of this Act.



Part six of Act No. 147/2002 Sb.



Transitional provisions



(1) applications for the granting of credentials for laboratory tests, the quality of feed,

additives and premixtures according to feed ^ 7), or request for

grant credentials to take samples of soil and chemical analyses for

the purpose of agrochemického testing of agricultural land according to the law on

fertilisers ^ 8), filed before the date of entry into force of this Act shall be

be deemed to grant you permission under this Act.



(2) the credentials granted by the Institute for laboratory tests, the quality of feed,

additives and premixtures according to feed ^ 7) and credentials

granted by the Institute of soil sampling and chemical analysis of them for

the purpose of agrochemického testing of agricultural land according to the law on

fertilisers ^ 8) before the date of entry into force of this Act shall be construed as

permissions granted under this Act.



8) section 10 of Act No. 157/1998 Coll., as amended.



7) section 17 of Act No. 91/1996 Coll., as amended.



Article. (III) Act No. 21/2004 Sb.



Transitional provisions



1. Entrepreneurs who produce feedingstuffs with the use of supplementary feed and

they are used for the need for animal primary production, but do not expose them to

circulation, are required to report this fact to the institution under section 8b of law No.

91/1996 Coll., as amended by this Act, not later than 6 months from the date of

entry into force of this Act.



2. The provisions of § 3a of Act No. 91/1996 Coll., as amended by this Act,

shall expire on the date of the Treaty of accession of the Czech Republic

The European Union enters into force.



Article. (II) Act No. 214/2007 Sb.



Transitional provisions



1. registration of importers, suppliers and distributors, in accordance with

the existing legislation is considered as a registration under the Act No.

91/1996 Coll., on feedstuffs, in the version in force from the date of entry into force of

This Act, to the extent that the importer, supplier or

the Distributor ran the effective date of this Act.



2. feed business operators ' production facilities authorised under

the existing legislation shall be regarded as approved under Act No.

91/1996 Coll., on feedstuffs, in the version in force from the date of entry into force of

of this Act. Feed business operators ' production facilities

registered in accordance with the existing legislation shall be considered as

registered under this Act.



3. Finally the executor to the effective date of this Act,

shall be terminated in accordance with the existing legislation.



4. the operator is obliged to the deadline set out in the article. 18 paragraph 1. 3 of regulation

The European Parliament and of the Council (EC) No 183/2005 and on a form issued by the

the Institute make a declaration of compliance with the requirements laid down in this

provision.



Article. (II) Act No. 33/2010 Sb.



Transitional provision



Proceedings initiated before the date of entry into force of this law, and to this

the day hedge contingent exposures are completed and the rights and obligations related to

assessed according to the Act No. 91/1996 Coll., on feedstuffs, as amended effective to

the effective date of this Act.



1) Article. 6 of Commission Directive 98/51/EC of 9 December 1999. July 1998, which

lays down certain measures for implementing Council Directive 95/69/EC

lays down the conditions and arrangements for approving and registering certain

establishments and intermediaries operating in the animal feed sector.



Directive of the European Parliament and of the Council 2002/32/EC of 7 September 2004. May 2002

on undesirable substances in animal feed, as amended.



Commission Directive 2002/63/EC of 11 December 1997. July 2002 laying down the

Community methods of sampling for the official control of residues

pesticides in products of plant and animal origin and on their

surface and repealing Directive 79/700/EEC.



Commission Directive 2008/39/EC of 5 July 2004. March 2008 laying down

a list of intended uses of animal feedingstuffs for particular nutritional purposes, as amended.



1A) European Parliament and Council Regulation (EC) 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.



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 (EC) No 1774/2002 of 3 October 2002. October

2002 laying down health rules for animal by-products

origin not intended for human consumption, as amended.



European Parliament and Council Regulation (EC) No 1829/2003 of 22 July 2003. September

2003 on genetically modified food and feed.



European Parliament and Council Regulation (EC) no 1830/2003 of 22 July 2003. September

2003 concerning the traceability and labelling of genetically modified organisms

and the traceability of food and feed products produced from genetically

modified organisms and amending Directive 2001/18/EC.



European Parliament and Council Regulation (EC) no 1831/2003 of 22 July 2003. September

2003 on additives used in animal nutrition.



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 183/2005 of 12 April 2005. January

2005 laying down requirements for feed hygiene.



European Parliament and Council Regulation (EC) No 396/2005 of 23 November 2005. February

2005 on maximum residue levels of pesticides in food and feed

plant and animal origin and on their surface and amending Directive

Council 91/414/EEC, as amended.



Commission Regulation (EC) no 429/2008 of 25 June. April 2008 implementing

rules for the regulation of the European Parliament and of the Council (EC) no 1831/2003,

with regard to the preparation and submission of applications and the evaluation and authorisation of

the additives.



Commission Regulation No 158/2009 of 27 May. January 2009 laying down

methods of sampling and laboratory testing for official controls

feed.



European Parliament and Council Regulation (EC) no 767/2009 of 13 July.

July 2009 on the placing on the market and use of feed, amending Regulation (EC)

No 1831/2003 and repealing Council Directive 79/373/EEC, Commission directive

80/511/EEC, Council Directive 82/471/EEC, 83/228/EEC, 93/74/EEC, 93/113/EC and

96/25/EC and Commission decision 2004/217/EC.



Commission Regulation (EC) no 669/2009 of 24 September. July 2009 laying

performs a regulation of the European Parliament and of the Council (EC) No 882/2004, if

as for the reinforced official controls on imports of certain feed and food of another

than animal origin and amending Decision 2006/504/EC, in

the texts of Commission Regulation (EU) No 212/2010.



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).



Commission Regulation (EC) no 1135/2009 of 25 June. November 2009

laying down special conditions for the import of certain products originating in or

sent from China, and repealing Commission decision No.

2008/798/EC.



Commission Regulation (EU) No 257/2010 of 25 March. March 2010 laying

imposing special conditions for the import of guar gum originating in or

consigned from India due to the risks of contamination and pentachlorfenolem

dioxins and repeals decision No 2008/352/EC.



1B) Article. 2 (2). 2 (a). a) European Parliament and Council Regulation (EC)

No 1831/2003.



1 c) Article. 2 (2). 2 (a). e) European Parliament and Council Regulation (EC)

No 1831/2003.



1 d) Act No. 147/2002 Coll., on the central control and testing Institute

Agriculture and amending certain related laws (the law on the Central

inspection and test Institute of agriculture), as amended

regulations.



1E) Act No. 167/1999 Coll., on health care and on amendments to certain

related laws (health law), as amended.



2) Act No. 79/1997 Coll., on pharmaceuticals and on amendments and additions to some

related laws, as amended.



2A) Act No. 167/1999 Coll., on health care and on amendments to certain

related laws (health law), as amended.



2B) Article. 2 paragraph 1 of the regulation of the European Parliament and of the Council (EC) No 882/2004.



2 c) Article. 3 (b). b) European Parliament and Council Regulation (EC) No.

183/2005.



Article. 3 points 5 and 6 of the regulation of the European Parliament and of the Council (EC) No.

178/2002.



2D) § 3 (1). 1 (b). o) Act No. 167/1999 Coll., as amended

regulations.



3) § 19 para. 2 of the Act No. 168/1999 Coll.



3A) European Parliament and Council Regulation (EC) No 1829/2003.




3B), for example, Commission Regulation (EC) No 102/2009 concerning the permanent authorisation of

the additive, Commission Regulation (EC) No 214/2009 amending

Regulation (EC) no 1800/2004 as regards the terms of the authorisation

substance Cycostat 66 G, Commission Regulation (EC) No 554/2008 concerning the authorisation of

6-phytase (Quantum Phytase) as a feed additive.



3 c) European Parliament and Council Regulation (EC) No 183/2005.



4) Article. 10, paragraph 1. 1 European Parliament and Council Regulation (EC) No.

183/2005.



4A) European Parliament and Council Regulation (EC) No 183/2005 of 12 April 2005.

January 2005 laying down requirements for feed hygiene.



4B) Article. 3 European Parliament and Council Regulation (EC) No 183/2005.



5) Article. 3 (b). d) European Parliament and Council Regulation (EC) No.

183/2005.



5A) Article. 18 paragraph 1. 3 European Parliament and Council Regulation (EC) No.

183/2005.



5B) Act No 449/2001 Coll., on game management, as amended.



5 c) § 49 paragraph 1. 1 (b). j) Act No. 167/1999 Coll., as amended

regulations.



6) § 17 of the Act No. 513/1991 Coll., the commercial code, as amended

regulations.



7) Article. 19 of the European Parliament and Council Regulation (EC) No 183/2005.



8) Article. 14 to 16, art. 18 paragraph 1. 3 regulation of the European Parliament and of the Council

(EC) No 183/2005.



8A) Act No 246/1992 Coll., on the protection of animals against cruelty, as amended by

amended.



9) Article. 9. 2 and article. 18 paragraph 1. 2 regulation of the European Parliament and of the Council

(EC) No 183/2005.



9B) 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.



9 c) annexes I, II and III of European Parliament and Council Regulation (EC) No.

183/2005.



9 d) Article. 6 (1). 1 European Parliament and Council Regulation (EC) No.

183/2005.



for example, article 9 quinquies). 15 and 20 of the regulation of the European Parliament and of the Council (EC) No.

178/2002.



9f) European Parliament and Council Regulation (EC) No 183/2005.



9 g) Annex I, part A, point 3 of the regulation of the European Parliament and of the Council (EC)

No 183/2005.



9 h) Article. 19 para. 4 European Parliament and Council Regulation (EC) No.

183/2005.



9i) Article. 16 of the European Parliament and Council Regulation (EC) no 1831/2003.



10) for example, § 39 of Act No. 167/1999 Coll., Act No. 20/1966 Coll. on care

about the health of the people, as amended, section 57 of the 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,

in the wording of later regulations.



10A) Act No. 125/1997 Coll., on waste, as amended.



Act No. 157/1998 Coll., on fertilisers, soil conditioners,

auxiliary plant products and substrates and agrochemical

testing of agricultural soils (fertilisers).



10B) for example, regulation of the European Parliament and of the Council (EC) No 999/2001

of 22 March. May 2001 laying down rules for the prevention, control and

eradication of certain transmissible sponginoformních encephalopathies,

as amended, the European Parliament and of the Council Regulation (EC) No 1829/2003

of 22 March. September 2003 on genetically modified food and

feedingstuffs, as amended, regulation of the European Parliament and of the Council No.

1830/2003 of 22 July 2003. September 2003 concerning the traceability and labelling of

genetically modified organisms and the traceability of food and feed

produced from genetically modified organisms and amending Directive

2001/18/EC, as amended, regulation of the European Parliament and of the Council (EC)

No 1831/2003 of 22 July 2003. September 2003 on additives used in

animal nutrition, regulation of the European Parliament and of the Council (EC) No 183/2005.



10 c) European Parliament and Council Regulation (EC) no 1831/2003.



Annex I and IV of the regulation of the European Parliament and of the Council (EC) No 999/2001,

, as amended.



10 d) Article. 5 European Parliament and Council Regulation (EC) no 1831/2003.



10E) Annex I to III of European Parliament and Council Regulation (EC) No.

1831/2003.



Article 10F). 54 European Parliament and Council Regulation (EC) No 882/2004 of

29 April 2004. April 2004 on official controls performed for the purpose of authentication

compliance with the legislation on feed and food and provisions on

animal health and animal welfare, as amended.



11) Article. 2 regulation of the European Parliament and of the Council (EC) No 882/2004.



12) Act No. 337/1992 Coll., on administration of taxes and fees, as amended by

amended.



12A) Article. 28 European Parliament and Council Regulation (EC) No 882/2004.



12 c) Act No. 110/1997 Coll. on foodstuffs and tobacco products and

amendments to some related laws, as amended

regulations.



13) Article. 11 of European Parliament and Council Regulation (EC) No 882/2004.



Article 13 c). 5 (3). 6 European Parliament and Council Regulation (EC) No.

183/2005.



13E) European Parliament and Council Regulation (EC) no 1831/2003.



Commission Regulation (EC) no 429/2008.



14) Ministry of Agriculture of the CZECH REPUBLIC Decree No 413/1991 Coll., on registration of

some species feed their suppliers of professional and State control.



Decree of the Ministry of Agriculture of the CZECH REPUBLIC No. 362/1992 Coll., on the manufacture and

composition of compound feedingstuffs, as amended by decrees no. 258/1993 Coll. and no 190/1995

SB.



16) for example, annex I of Commission Regulation (EC) no 669/2009, article. 3

Commission Regulation (EC) no 1135/2009. 1 Commission Regulation (EU) No.

258/2010.



17) Article. 19 of the European Parliament and Council Regulation (EC) No 183/2005.



18) Commission Directive 2002/63/EC.



Article. 7 and 11 of European Parliament and Council Regulation (EC) No 882/2004.



Commission Regulation (EC) No 152/2009.



19) Article. 3 (2). 1 European Parliament and Council Regulation (EC) No.

767/2009.



Article. 4 (4). 1 European Parliament and Council Regulation (EC) no 767/2009.



20) Article. 5 (3). 6 European Parliament and Council Regulation (EC) No.

183/2005.



21) for example, European Parliament and Council Regulation (EC) no 767/2009,

European Parliament and Council Regulation (EC) no 1831/2003.



22) Act No 634/2004 Coll., on administrative fees, as amended

regulations.



23) Decree No. 221/2002 Coll., laying down a scale of reimbursement

for training and test activities pursued within the scope of the Central

control and testing Institute of agricultural, as amended

regulations.