281/2002 Sb.
LAW
of 30 March 2004. May 2002
on certain measures connected with the prohibition of Bacteriological
(Biological) and Toxin Weapons and on the change of the Trade Licensing Act
Change: 186/2004 Sb.
Change: 413/2005 Sb.
Change: 296/2007 Sb.
Change: 124/2008 Sb.
Change: 223/2009 Sb.
Change: 227/2009 Sb.
Change: 64/2014 Sb.
Parliament has passed the following Act of the Czech Republic:
PART THE FIRST
MEASURES RELATED TO THE PROHIBITION OF BACTERIOLOGICAL (BIOLOGICAL) AND
TOXIN WEAPONS CONVENTION
TITLE I OF THE
BASIC PROVISIONS
§ 1
The subject of the edit
This Act regulates the
and) the rights and obligations of natural and legal persons related with
the prohibition of the development, production, Stockpiling and use of Bacteriological
(Biological) and Toxin Weapons and on their destruction, with the handling of
established high-risk and hazardous biological agents and toxins,
that can be diverted to the violation of the prohibition of Bacteriological
(Biological) and Toxin Weapons, and
(b)) performance of State administration in this area.
§ 2
The definition of certain concepts
For the purposes of this Act, means the
and the bacteriological (Biological)) and the toxinovými arms
1. weapons whose destructive effect is based on the properties of
biological agents and toxins that damage the health of people or animals
or the cause of their death or damage the plants or cause
economic damage,
2. materials that contain biological agents or toxins of any
origin or production, and their types and quantities
do not respond to the need for their use for prophylactic, protective or
other peaceful purposes,
3. any equipment, apparatus, or methods of dissemination of the proposed
to use and filled with such biological agents or toxins, or
weapons that have special design form suitable for filling and
the use of such biological agents or toxins for hostile purposes
or in armed conflict; the same is true for biological vectors
agents deliberately infected to hostile purposes or for use in the
armed conflict,
(b) any biological agent) organism natural and modified,
whose deliberate use can cause death, disease, or zneschopnění
people and animals, or that may cause death or harm to plants,
(c)) resulting from any toxin substance in organisms, including microorganisms,
animals or plants of any manufacturing method, natural or
chemically modified substance, or syntetizovaná, which can cause
death, illness or otherwise harm people, animals or plants,
d) high-risk biological agents and toxins of such biological
agents and toxins that have such features or capabilities that can
be used as a weapon, and the list is determined by Decree,
e-risk biological agents) and toxins biological agents and toxins,
which is possible under certain conditions to dispose of, and the list is
established by Decree,
(f) the level of technical security equipment) BL 3 the WHO and the WHO, BL 4 space
in particular, room, rooms, laboratories, summary, or other building or
buildings meeting the requirements of the appropriate level of technical security
adjusted in accordance with ČSN-EN 12128 Biotechnology-laboratories for research,
development and analysis of the security level of microbiological laboratories, zone
risk areas and the technical safety requirements,
g) diagnostic equipment a device that tests the samples for the purposes of
diagnosis, clinical or subclinical latent infection or
intoxikací people, animals or plants, or for purposes of analysis
microbial toxin or contamination of food, water, soil and air
through the detection, isolation or identification of microbial or
other biological agents or toxins,
h) vaccine preparations, including fatalities, debilitated, or otherwise
modified live micro-organisms or the components obtained from
micro-organisms, including the recognized toxins and nucleic acids, which
After the introduction of any path in the body of man or animal in them
induce a specific immune response to prevent or protect against
infekčnímu disease or intoxication and are generally effective and safe
for people or animals,
even the production of biological agents) the cultivation of reproducible by any
resources, synthesis, biosynthesis, extraction of nereprodukovatelných
biological agents or toxins,
j) aerobiologií study or work with aerosols containing biological
agents and toxins, or their imitators in the device or in the free
space,
imitators of biological agents) and toxins biological, chemical substances
or other origin, which due to its characteristics
used for the research of properties of biological agents or toxins,
l) management with the high-risk, and risk
biological agents and toxins of their development, production, use, acquisition,
the possession, import, export, transport and destruction; treatment of established
high-risk and hazardous biological agents and toxins is not running
According to the law on the free movement of services,
written declarations report m) of the prescribed information on high-risk and
risk biological agents and toxins and of objects and devices
referred to in points (d), (e))) and (n)), in which they are treated by,
n) device device used for the development, production, Stockpiling and use
of Bacteriological (Biological) and Toxin Weapons, in particular
aerosol Chamber, static, dynamic, explosive, fermenters,
bioreactors, centrifuges, dryers, sterilization, stripping, drum,
anaerobic storage boxes, mikrozapouzdřování equipment, equipment for
automatic sequential processing of deoxyribonucleic acid (DNA) and
Automatic synthesis of DNA, sequential processing, synthesis of peptides
peptides, autoclaves, incubators, chambers for the breeding of insects and carriers,
about) international inspector authorized representative of international organizations,
carrying out inspection activities for the purpose of monitoring the implementation of the Convention on the
the prohibition of the development, production and Stockpiling of Bacteriological
(Biological) and Toxin Weapons and on their destruction (hereinafter referred to as
"The Convention"), "^ 1")
p) prohibited information information directly to allow the development or the production of
of Bacteriological (Biological) or toxin weapons, highly
risk agents or toxins,
r) handling of prohibited information gathering, or for
in return the provision or disclosure of restricted information.
§ 3
State administration in the field of the prohibition of Bacteriological
(Biological) and Toxin Weapons
(1) the State administration in the field of the prohibition of Bacteriological
(Biological) and toxin weapons shall be exercised by the State Office for nuclear
Safety (hereinafter "the Office"), which at the same time pursues the scope
the national authority for the implementation of the Convention.
(2) the Office of the
and) shall exercise supervision of compliance with the prohibition of Bacteriological
(Biological) and Toxin Weapons
(b) shall exercise supervision over the management) with high risk and risk
biological agents and toxins in accordance with this Act,
(c)), amended and repealed the decision on authorisation to dealing with high
risk biological agents and toxins in accordance with this Act,
(d)) keeps records of
1. the holder of a permit issued under this Act, and
2. natural and legal persons that handle risk
biological agents or toxins under section 17,
(e)), the registration of high-risk and high-risk biological agents,
toxins and equipment and draw up a declaration about them.
(3) in supervisory activities uses the Office next to your device and
reference laboratories for high risk and the risk of biological agents and
toxins, operated by the Ministry of health and the Ministry of Defense.
TITLE II
THE PROHIBITION OF BACTERIOLOGICAL (BIOLOGICAL) AND TOXIN WEAPONS AND EQUIPMENT
ON THEIR PRODUCTION
§ 4
(1) the development, production, Stockpiling, possession, handling, use, consumption,
the import, export, transport, including transit, trading and other waste
Bacteriological (Biological) weapons and toxinovými and management
disabled information are prohibited.
(2) the development, production, Stockpiling, possession, import, export, trading and other
disposal of equipment for the production of Bacteriological (Biological) or
toxin weapons and their means of delivery, or the design, construction and
the use of plants for their production shall be prohibited.
§ 5
(1) Find the materials or things that you can believe, that can be
Bacteriological (Biological) weapons or toxinovou, or they can
contain high risk biological agents or toxins, as well as
suspicion about the treatment of the disabled information is each obliged to
immediately notify the police of the Czech Republic or to the competent territorial
and the Office of the public prosecutor's Office.
(2) For the discovery of the device shall be used mutatis mutandis the provisions of paragraph 1.
(3) the person who does not have a permit issued by the authority under section 6 (1). 1 and randomly
in its activities the isolates or detects high-risk biological agents
or toxins, is obliged to notify this fact to the Office.
(4) the Office shall provide the implementation of disposal of materials, goods and equipment
referred to in paragraphs 1 to 3. The costs borne by the State. This is without prejudice to
liability for damage under the specific legislation.
TITLE III
THE USE OF HIGH RISK BIOLOGICAL AGENTS AND TOXINS
§ 6
The management of high risk biological agents and toxins
(1) to dispose of high-risk biological agents and toxins on the territory of the
The Czech Republic can only be on the basis of authorisation issued by the Authority
and for industrial, agricultural), research, medical, pharmaceutical
and other peaceful purposes,
(b)) to the protective purposes directly related to the defence against the
Bacteriological (Biological) weapons or toxinovým
(c)) to prevent, identify, diagnose, and treat diseases, which are
caused by biological agents or toxins.
(2) a permit issued by the authority under this Act, do not replace the permit
issued in accordance with the specific legislation. ^ 2)
(3) every person who discovers the loss provided for high-risk biological
agents or toxins, or damage to the equipment, is obliged to notify this
the fact immediately to the Office.
section 7 of the
The conditions for the issue of permits to the management of high risk
biological agents and toxins
(1) the authorisation to the management of high risk biological agents and
toxins (hereinafter referred to as "permits"), the Office shall issue to the legal or natural person under the
the conditions that
and) legal person has its seat or a natural person who resides in the territory of the Czech
of the Republic,
(b)) of the person, which are statutory bodies or members of the statutory body
legal persons that authorisation is to be issued, they are eligible for legal
capacity and of good repute,
(c) appoint a responsible representative) of a legal entity, which is responsible for
the proper performance of all activities related to the permitted use;
responsible representative must be eligible for legal capacity, integrity and
competent, cannot be a member of the Supervisory Board, or else
the control body of the legal person; the function of a responsible representative of the
You can perform only one legal person,
(d)) a natural person who permit should be issued, and its responsible
Representative, if appointed, are eligible to legal capacity, integrity
and professionally qualified,
(e)) was cancelled the permit under section 12, paragraph. 3 (b). and (b))).
(2) compliance with the conditions referred to in paragraph 1 (b). and) is not required for
legal persons and natural persons are established with the stay on the territory of
a Member State of the European Union.
(3) a change in the facts referred to in paragraph 1 is a legal person shall be obliged to
notify the Office.
(4) the provisions of paragraph 1 and paragraph 2 shall be applied mutatis mutandis to the business
components of the State and its authorized staff.
§ 8
Integrity
(1) For an impeccable for the purpose of this law shall be considered as one who has not been
been sentenced for an offence committed through negligence, the
the merits of the activities related to the povolovanou, or of an offence
committed intentionally.
(2) a document authenticating the integrity is
and extract from) criminal record of the natural person, the person who is
a statutory body or a member of the statutory body, and excerpt from the register
The criminal record of the responsible representative, or
(b) a similar proof of good repute) issued by the competent authority of the Member
State of the European Union, which is a natural person, the statutory authority, the
responsibility of the statutory body or representative of a national; in
If the competent authorities of the State, such documents are not issued, they may be
replaced with a solemn statement made by the competent authority or
before a notary in the Member State of the European Union.
(3) in order to demonstrate the integrity Office's requests under the Special
the law ^ 2a) an extract from the criminal register. The request for
the release of the statement from the criminal register and the excerpt from the register Index
penalties shall be communicated in electronic form, in a way that allows
remote access.
§ 9
The competence of the
Competence for activities related to the management of highly
risk biological agents and toxins shall mean the duly completed
higher education studies in the study programme in the field
and 3 years experience in the field; range of study programmes in the field
the authority shall lay down the implementing legislation.
§ 10
The application for the grant of authorisation
(1) a written request for the granting of authorisation shall include the
and the business name or name), address, identification number of the person (hereinafter
"identification number") of a legal person, which asks for authorization,
name and last name, social security number, citizenship, permanent residence of a person
or persons who are the statutory body or its members,
(b) the natural person) for the first and last name, social security number, citizenship, and
residence, name and last name, social security number, citizenship and residency
the responsible representative, if appointed,
(c) the name of the high risk biological) agents or toxin, his
the amount, purpose and the treatment and final destination,
(d)) the purpose of the import or export of high-risk biological agents or
the toxins.
(2) a request for authorisation must be accompanied by the
and) proof competence of individuals and support
competence of responsible representatives,
(b)) the technical documentation, including the implementation of the plan of construction, specifications
facilities and equipment installed and the kolaudačním decision,
(c) an approved body) reporting of public health protection by the competent
in the place of the activity under a special legal regulation, ^ 3)
(d)) that the legal person has not been issued
the decision of the bankruptcy or insolvency was rejected because the
the assets of this person is not sufficient to cover the costs of the insolvency proceedings,
(e) the other documents referred to in the request) of the Office.
(f) if the applicant's) integrity of osvědčována document pursuant to section 8 (2). 2
(a). (b)), this document must be attached to the application.
§ 11
The decision on issue of authorisation
(1) the authority shall, in proceedings for the issue of authorisation, independently of the
proceedings against any other administrative authority. The applicant is the sole party to
the proceedings.
(2) the Office shall decide on the issue of the permit within 90 days of the initiation of the
the proceedings.
(3) in a decision on the issue of the permit shall indicate the Office
and the business name or name), registered office and identification number of the legal
the person applying for the permit, and the first and last name, social security number, Permanent
residence of the person or persons who are the statutory body or a member of the,
(b)) and last name, social security number and residence of a natural person and the name and
last name, social security number and residence of the responsible representative, if
appointed,
(c) the subject-matter and scope of the authorization) to the management,
d) type and quantity of high risk biological agents or toxins,
You can dispose of,
e) conditions under which can be used with high-risk biological agents or
the toxins.
(4) a permit is not required for rescue operations, aiming to avert
emergency or winding-up work towards the Elimination of
the effects caused by extraordinary events; ^ 4) complete
report immediately to the Office.
(5) the application for authorisation shall be refused if the applicant fails to comply with the terms of the
This law, or would have exceeded the total number of highly
the risk of a biological agent or toxin to a specific period on the territory of the
The Czech Republic; the total amount of high risk biological agents
or the toxin for a certain period in the territory of the Czech Republic, which must not be
exceeded, the Office shall lay down the implementing legislation.
§ 12
Changing conditions, change, cancellation and termination of authorisation
(1) without the prior written consent of the authority, issued on the basis
the application of the holder of the authorisation, shall be no changes made to the
device or other technical or organisational changes important in terms of
of this law.
(2) the authority may decide to change
and) on the basis of a reasoned request of the authorisation holder,
(b)) If you have to change the facts on the basis of which the authorization was
released.
(3) the Office shall cancel the authorization if
and its holder is won) on the basis of false or incomplete information, the
(b) the authorisation holder fails to) the obligations laid down in this law or
does not remove the shortcomings detected by the Office,
(c) the responsible representative) for the holder of the authorization ceases to carry out their
the function and the holder of the authorisation shall forthwith neustanovil new responsible
the representative asked the Office of change and authorization,
(d)) the holder no longer fulfils the conditions for its issue or
asked in writing of its cancellation.
(4) the authorisation shall expire
and the date of dissolution of a legal person) or for natural persons, or death, or
a statement from the dead,
(b)) Declaration of bankruptcy.
(5) a decision on the amendment or cancellation of the permit does not have suspensory effect.
section 13
Obligations of permit holders
In particular, the authorisation-holder shall be obliged to
and dispose of high-risk) biological agents and toxins only in
the range specified in the permit,
(b)) to deal with high-risk biological agents and toxins, so that
It could not be misused or stolen,
(c)) to submit the Declaration within the time limits of the Office,
(d) allow the input to the device), to conduct a briefing on activities
currently held in the device, the safety measures necessary for
the performance of the audit activities of the Office of international inspectors and inspectors
persons invited by the Office,
(e) the location of the monitoring inspectors) to allow devices to monitor
high risk biological agents and toxins and remove samples for
analysis,
(f)) without undue delay, notify the authority of the initiation of the insolvency
the proceedings.
§ 13a
Transport
Transport of high risk biological agents or toxins and risk
biological agents or toxins can be only in containers and in a manner
laid down by a special law. ^ 5a)
§ 14
Exports and imports of high risk biological agents and toxins
(1) the Export from the territory of the Czech Republic and imported on the territory of the Czech Republic
high risk biological agents and toxins can only the holder of the authorization.
This authorisation does not replace a licence issued under a special rule
^ 6) of the code.
(2) the export of high risk biological agents and toxins by the holder
the permit is possible only in the Member States of the Convention, and only for the purposes described
in section 6.
(3) importation of high risk biological agents and toxins by the holder
the permit is possible only from the Member States of the Convention, and only for the purposes described
in section 6.
(4) exports and imports of high risk biological agents and toxins in the form of
mail addressed to úschovního places, customs warehouse, free
a customs warehouse, free zone or to persons other than
It is stated in the authorization, is prohibited.
(5) the holder of a permit under section 11 shall ensure that a person who carries out the
transport of high-risk biological agents or toxins in the vicinity
the territory of the Czech Republic or in the territory of the Czech Republic, the Customs Office when
implementation of surveillance ^ 6a) or in the implementation of control activities in transport
high risk biological agents or toxins
and submit a certified copy of the relevant) permit Office,
(b)) in writing of their reported to the input or output from the territory of the Czech Republic.
The Declaration must contain the identification data of the holder, the name and
the quantity transported of high-risk biological agents or
toxins, identification of the beneficiaries of the high risk of biological
agents and toxins, the name of the State in which the exportation has been effected or from
which has to be made, and the date of importation of the input or output,
(c) submit a certified copy of the licence) issued in accordance with a special legislative
code ^ 6b), or if the license is not required by law,
1. a contract concluded between the exporter or importer and the
the foreign contractual partner with the exact specifications of the controlled
high risk biological agents or toxins, including their
the quantity,
2. the export declaration the foreign end user that the high
the risk of biological agents or toxins will not be used for the production or
the development of biological weapons, with the specific purpose of their
the use,
3. the export declaration that the high risk biological agents or toxins
will not be re-exported without the consent of the country of the exporter,
4. when the import statement with the written commitment of the final user, that
the specified high risk biological agents or toxins shall be
used only for the permitted purpose.
§ 15
cancelled
section 16 of the
Registration and Declaration of high risk biological agents and toxins
(1) the holder of the authorization shall keep a record of
high-risk biological agents or toxins, and on request
submit to the Office; records are kept for 10 years from the end of the authorisation to
the management of high risk biological agents or toxins.
(2) the register shall be kept by the device in which it is registered
the activities carried out by each of the species and quantity of high risk
biological agents or toxins.
(3) in the demise or cancellation of a permit is a permit holder shall be obliged to
submit to the Office a register on the management of high risk
biological agents or toxins.
(4) the permit holder must submit to the Office a declaration for the past
calendar year not later than 31 December 2006. January of the following year and
the projected figures for the following calendar year to 31. August of
of the year.
(5) the Declaration shall contain the
and the business name or name), address, identification number of a legal
persons first and last name, social security number, citizenship, residence of the person
or persons who are the statutory body or its members, or
name and last name, social security number, citizenship and residence of a natural person,
b) type and quantity of high risk biological agents or toxins,
(c)), in which the declared activity is carried out.
(6) details of the registration and the data contained in the Declaration
the authority shall lay down the implementing legislation.
TITLE IV
THE USE OF HIGH-RISK BIOLOGICAL AGENTS AND TOXINS
§ 17
Risk biological agents and toxins
(1) a natural or legal person who is treated with biological risk
agents or toxins as referred to in section 2 (a). (e)), is required to notify the Office of
the form of the Declaration data for the previous calendar year to 31. January of the year
the projected figures for the following and the following calendar year always
until 31 December 2006. in August of that year.
(2) the Declaration shall contain the
and the business name or name), address, identification number of a legal
the person having the obligation to declare and name and last name, social security number,
citizenship, residence of the person or persons who are its statutory
body or its members, or name, last name, social security number, the State
citizenship, residence of a natural person having the obligation under
paragraph 1,
b) type and quantity of high-risk biological agents or toxins,
(c)), in which they have reported the activity to take place.
(3) in the event that a natural or legal person proposes to dispose of for the first time
risk biological agents or toxins, or in the event that there is a
change the anticipated data for the following calendar year, the
the person required to fulfil the obligation of notification within 14 days prior to the
treatment or changes.
(4) the obligation to declare applies to the installation of new equipment.
(5) in the event that there is a change of the anticipated data for the following
the calendar year is a natural or legal person referred to in § 17 paragraph. 1
required to comply with the notification obligation within 14 days prior to its implementation.
(6) For the registration of high-risk biological agents and toxins shall apply mutatis mutandis
the provisions of section 16.
(7) import and export risk biological agents and toxins is only possible
on the basis of, to the extent and under the conditions laid down by specific legal
6. ^ ^)
(8) the legal or natural person shall ensure that the person who carries out the
the transport of high-risk biological agents or toxins from the territory or on the territory of the
The Czech Republic, the Customs Office in the implementation of customs supervision ^ 6a) or
in the implementation of control activities in the transportation risk biological
agents or toxins
and a certified copy of the Declaration) presented pursuant to paragraph 1 or 3 confirmed
The Office,
(b)) in writing of their reported to the input or output from the territory of the Czech Republic.
The Declaration must contain the identification data of the legal or natural
the person, the name and quantity of the transported risk biological agents and
the toxins, the identification data on the risk of biological agents and
the toxins, the name of the State in which the exportation has been effected or from which
has to be made, and the date of importation of the input or output,
(c) submit a certified copy of the licence) issued in accordance with a special legislative
code ^ 6b), or if the license is not required by law, the contract of purchase
concluded between the exporter or importer and the foreign contracting
partner with the precision specifying the controlled biological risk
agents or toxins, including their quantity, and with an indication of the specific purpose
their use.
THE HEAD OF THE
SUPERVISION OF COMPLIANCE WITH THE LAW
section 18
Supervision
(1) the authority shall exercise the supervision of compliance with this Act and other
the legislation issued on the basis of (hereinafter referred to as "surveillance").
(2) the Office shall monitor
and the holder of the authorization) to the management of high risk biological agents
or toxins under section 11,
(b)) a person treating hazardous biological agents or toxins under the
section 17, or
(c)) of the person for which there is reasonable suspicion that the handling of a highly
risk biological agents or toxins without permission.
(3) the Supervision Authority shall be exercised by the President and inspectors of the Office (hereinafter referred to as
"inspectors"); the inspectors appointed and recalled by the President of the Office.
§ 19
Cooperation with ministries and other administrative authorities
(1) the ministries and other administrative authorities shall inform the Office of the
the occurrence of epidemics and diseases in humans, animals and plants, if it is suspected,
that spill of high-risk biological agents or toxins or
their misuse, and within its scope of action to carry out their
early detection and to restrict their release.
(2) the Customs authorities shall notify the Office of the information referred to in section 14, paragraph. 5 and § 17 paragraph.
8 in January and July for the preceding six months. If it finds
the Customs authorities of the shortcomings in the activities of the persons inspected under section 14 or
§ 17, carried a high risk or at risk
biological agents or toxins to detain and of this fact without delay to the
inform the Office.
section 20
Measures to remedy the
Detects if the President and inspectors of the shortcomings in the activities of the
the controlled persons, are entitled to according to the nature of the observed lack of
and) require that the controlled person within a specified period fashion
remedy, or
(b) the controlled person) to save the implementation of technical checks, inspections or
tests of operational capacity of the device, its parts, or
their files.
section 21
Fines and other penalties and saving
(1) the authority may impose a fine of up to
and 100 0000 0000 Czk), who violated the prohibition of the development, production and Stockpiling and
the use of Bacteriological (Biological) and Toxin Weapons
(b) $ 50 0000 0000) a person who without the permission of the authority handling
set high risk biological agents and toxins,
(c) the holder of the authorization) 5 0000 0000 Czk for violation of the obligations referred to in section
16 or the prohibition in section 12, paragraph. 1,
(d)) 10 0000 0000 Czk a person for violation of the obligations referred to in section 14,
(e)) 5 0000 0000 Czk a person for violation of the obligations referred to in section 5 (3). 3
or section 17,
(f)) 200 000 Eur for persons who are the statutory body or its members, and
the responsible representatives and 100 USD staff checked the person for
distortion or concealment of facts important for the performance of supervision or
non-participation in the control, or to people that did not meet
the obligation referred to in section 5 (3). 1 and 2.
(2) a fine may be imposed within 3 years from the date on which the Office has detected a violation of the
obligations, but within 10 years from the date on which the breach of the obligations
has occurred.
(3) in determining the amount of the fine to take account of the seriousness, importance and time
the duration of the infringement and to the extent caused by the consequences of the
timeliness and effective synergy of troubleshooting; in the case where
remedy immediately, when violations were found
obligations and the authority was granted effective synergy and to avoid
the damage to persons or to the environment, the Office may, from
fines waived.
(4) the Fines collected and enforced by the Authority. The fines are the income of the State budget.
(5) for the recovery of fines imposed as specific legal
legislation. ^ 9)
(6) the imposition of the fines referred to in paragraph 1 shall not prevent the procedure under section 12, paragraph. 3
(a). and (b))) and § 20.
TITLE VI OF THE
THE PROVISIONS OF THE COMMON, TRANSITIONAL AND FINAL
section 22
(1) the Office shall issue decrees for the implementation of section 2 (a). (d)), and (e)), § 9, § 11 (1). 5
and section 16, paragraph. 6.
(2) in proceedings under this Act shall proceed according to the administrative code,
If this law provides otherwise.
(3) an application for the grant of authorisation, as well as the fulfilment of the obligation to
the presentation of a declaration under this Act are legal and natural
persons who operate the operations covered by this law referred to in
the existing legislation, are obliged to transmit to the Office no later than within 1 month from the date of
date of entry into force of this Act.
(4) the fulfilment of the obligations of the Declaration is retained the right to dispose of the
risk biological agents and toxins.
(5) a legal person or a natural person who, on the date of entry into force of
This Act treated with high-risk biological agents or
high-risk toxins when doing business on the basis of trade licence
permissions, you may do so for a maximum of 6 months from the date of entry into force of
of this law.
(6) a legal person or a natural person who, on the date of entry into force of
This Act treated with biological agents or risk
toxins in the business on the basis of business, can
do continue, if within 14 days from the date of entry into force of this Act
fulfil the obligation under section 17.
PART THE SECOND
Amendment to the Trade Licensing Act
section 23
In Act No 455/1991 Coll., on trades (trade licensing
Act), as amended by Act No. 229/1992 Coll., Act No. 591/1992 Coll., Act
No 600/1992 Coll., Act No. 273/1993 Coll., Act No. 303/1993 Coll., Act
No 38/1994 Coll., Act No. 42/1994 Coll., the Act No. 136/1994 Coll., Act
No 200/1994 Coll., Act No. 237/1995 Coll., Act No. 283/1995 Coll., Act
No 94/1996 Coll., Act No. 95/1996 Coll., Act No. 147/1996 Coll., Act
No. 19/1997 Coll., Act No. 49/1997 Coll., Act No. 61/1997 Coll., Act No.
79/1997 Coll., Act No. 217/1997 Coll., Act No. 280/1997 Coll., Act No.
15/1998 Coll., Act No. 83/1998 Coll., Act No. 157/1998 Coll., Act No.
167/1998 Coll., Act No. 159/1999 Coll., Act No. 356/1999 Coll., Act No.
358/1999 Coll., Act No. 360/1999 Coll., Act No. 363/1999 Coll., Act No.
27/2000 Coll., Act No. 29/2000 Coll., Act No. 121/2000 Coll., Act No.
122/2000 Coll., Act No. 121/2000 Coll., Act No. 121/2000 Coll., Act No.
149/2000 Coll., Act No. 151/2000 Coll., Act No. 158/2000 Coll., Act No.
247/2000 Coll., Act No. 249/2000 Coll., Act No. 258/2000 Coll., Act No.
309/2000 Coll., Act No. 367/2000 Coll., Act No. 406/2000 Coll., Act No.
458/2000 Coll., Act No. 61/2001 Coll., Act No. 100/2001 Coll., Act No.
120/2001 Coll., Act No. 164/2001 Coll., Act No. 257/2001 Coll., Act No.
274/2001 Coll., Act No. 477/2001 Coll., Act No. 478/2001 Coll., Act No.
501/2001 Coll., Act No. 86/2002 Coll., Act No. 119/2002 Coll. and Act No.
174/2002 Coll., in section 3, paragraph 3. 3 at the end of the letter ae) dot is replaced by
the comma and the following point af), including footnotes, no.
h 23 m) is added:
"af) management of high risk and a risk to biological agents and
toxin. ^ h 23 m)
h 23 m) Act No. 281/2002, on certain measures connected with the
the prohibition of Bacteriological (Biological) and Toxin Weapons and on an amendment
the Trade Licensing Act. ".
PART THE THIRD
The EFFECTIVENESS of the
section 24
This Act shall take effect on the date of its publication, with the exception of the provisions of section 7 of the
paragraph. 2 and § 8 paragraph. 2 (a). (b)), which shall take effect on the date of entry
the Treaty of accession of the Czech Republic to the European Union.
Klaus r.
Havel in r.
in the from the. r. Rychetský in
Selected provisions of the novel
Article. XLV of law No 223/2009 Sb.
The transitional provisions of the
The proceedings initiated before the date of entry into force of this law, and to this
the unfinished March completes and the rights and obligations related to
be assessed in accordance with the existing legislation.
1) Convention on the prohibition of the development, production and Stockpiling of Bacteriological
(Biological) and Toxin Weapons and on their destruction under the famous No.
96/1975 Coll.
2) for example, Act No. 258/2000 Coll., on the protection of public health and the
changes to some related laws, as amended.
2A) Law No. 269/1994 Coll., on criminal records, as amended
regulations.
for example, 3) Decree No 89/2001 Coll., laying down the conditions for the
the classification of work into categories, limit values for biological indicators
exposure tests and requirements for the reporting of work with asbestos and biological
agents.
4) Law No. 239/2000 Coll., on the integrated rescue system and amending
Some laws.
5A), for example, the European Agreement concerning the international carriage of
of dangerous goods (ADR), adopted at Geneva on July 30. September 1957, the renowned
under no 4/1987 Coll., as amended, proclaimed under no. 159/1997
SB No. 186/1998 Coll., no. 54/1999 Coll., no 93/2000 Sb. m. s., no. 6/2002
SB. m. s. and no 65/2003 Coll. m. with.
6) Law No. 21/1997 Coll., on the control of the export and import of goods and technology
subject to international control regimes.
6a) Article. 4/13 of the Council Regulation (EEC) No 2913/92 of 12 October 1992. October 1992,
establishing the Community customs code, as amended.
6B), for example, law No. 21/1997 Coll., on the control of exports and imports of goods and
technologies subject to international control regimes.
for example, 9) Act No. 337/1992 Coll., on administration of taxes and fees, in the text of the
amended.
