Measures Related To The Apart And Of Biological Toxin Weapons

Original Language Title: Measures Related To The Prohibition Of Biological And Toxin Weapons

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Read the untranslated law here: https://portal.gov.cz/app/zakony/download?idBiblio=53594&nr=281~2F2002~20Sb.&ft=txt

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.