What is Act No. 350 / 2011 Coll.?

Act No. 350 / 2011 Coll., on Chemicals and Chemical Mixtures and on the Amendment of Certain Laws (Chemical Act) — Law on chemicals and chemical mixtures and on the modification of certain laws (chemical law).

When it became Act No. 350 / 2011 Coll. effectiveness?

Act No. 350 / 2011 Coll. became effective 01.01.2012.

Is Act No. 350 / 2011 Coll. still valid?

Yes, Act No. 350 / 2011 Coll. is still valid and effective.

How many times was it Act No. 350 / 2011 Coll. amended?

Act No. 350 / 2011 Coll. has 12 time versions of the text.

Act No. 350 / 2011 Coll. - Law on chemicals and chemical mixtures a...

350

THE LAW

of 27 October 2011

on chemicals and chemical mixtures and amending certain laws (chemical law)

Parliament has decided on this law of the Czech Republic:

ČÁST PRVNÍ

CHEMICAL SUBSTANCES AND CHEMICAL MIXES

HLAVA I

INTRODUCTORY PROVISIONS

§ 1

Subject matter

This law implements the relevant European Union1), builds upon the directly applicable European Union2) and provides for

(a) the rights and obligations of legal persons and business natural persons (hereinafter referred to as "person");

1. the manufacture, classification, testing of dangerous properties, packaging, labelling, placing on the market, use, export and import of chemical substances (3) (hereinafter referred to as "substance") or substances contained in mixtures or articles,

2. classification, testing of dangerous properties, packaging, labelling and marketing of chemical mixtures (4) (hereinafter referred to as "mixture") in the Czech Republic,

(b) good laboratory practice;

(c) the competence of the administrative authorities in ensuring protection against harmful effects of substances and mixtures.

§ 2

Scope of the law

(1) This law applies to substances, substances contained in a mixture or article and a mixture.

(2) The registration of substances and mixtures exported from the territory of the Czech Republic and imported into the territory of the Czech Republic shall also include plant protection products and plant protection aids in accordance with the legislation governing the placing on the market of plant protection products and plant protection aids (5). The obligation to notify under this Act also applies to authorised biocidal products under the law governing the supply of biocidal products on the market (6).

HLAVA III

CORRECT LABORATORY PRACTICE AND TESTING OF THE SUBSTANCE AND AMENDMENT

§ 17

Good laboratory practice

(1) Good laboratory practice means, for the purposes of this Act, a quality assurance system concerning the organisation process and the conditions under which non-clinical studies of the safety of the substance and mixture for health and the environment are planned, implemented, monitored, recorded, archived and reported.

(2) The implementing legislation lays down the principles of good laboratory practice (hereinafter referred to as "the principles').

Certificate of compliance

§ 18

(1) For the purposes of this Act and directly applicable European Union20, 21) only a person who has a certificate of compliance (hereinafter referred to as "certificate") shall carry out testing of the hazardous properties of a substance or mixture in the range of dangerous properties set out in Parts 3 and 4 of Annex I to Regulation (EC) No 1272 / 200821 of the European Parliament and of the Council.

(2) A certificate issued by a Member State of the Organisation for Economic Cooperation and Development under the provisions of the Organisation for Economic Cooperation and Development 22 shall be considered equivalent.

(3) A certificate issued by a Member State of the European Union shall be considered equivalent.

§ 19

(1) The certificate is issued by the Ministry of the Environment at the request of the person intending to test the hazardous properties of the substance or mixture.

(2) In addition to the general requirements, the application for certification must contain:

(a) the name of the head of the test facility;

(b) the number of the business authorisation; and

(c) a declaration of establishment of good laboratory practice, indicating the name and surname of the natural person responsible for the introduction.

(3) The certificate shall be accompanied by a report on the progress of the initial control of the testing equipment (hereinafter referred to as "the entry control ') carried out by the Ministry of the Environment established by the legal entity for the verification of the principles.

(4) Where the entry control shows that the person intending to test the hazardous properties of the substance or mixture complies with the principles, the Ministry of the Environment shall issue it with a certificate. Otherwise, it shall issue a decision rejecting the application.

(5) If, at the time of entry control in compliance with the principles, defects which do not have a significant impact on the quality of the test results of the hazardous properties of the substance or mixture are detected, the Ministry of the Environment shall interrupt the procedure and set a time limit for their removal.

§ 20

(1) Continuous verification of compliance with the principles of the holder of the certificate shall be carried out by the Ministry of the Environment set up by the legal person for verification of the principles by means of periodic checks on the testing equipment (hereinafter referred to as "periodic checks') or by audits of studies.

(2) The person who has applied for the certification or the holder of the certificate will allow the Ministry of the Environment set up by the legal person for verifying the principles of entry control, periodic checks and audits of studies to enter the land, premises and centres used for testing and provide information on compliance with the principles to the extent laid down in the implementing legislation.

(3) The data found during the entry control and periodic checks or audits of studies, other than the name of the laboratory, the quality of compliance with the principles and the date of the checks carried out shall be considered confidential and may only be provided to the authorities carrying out the control activity, by the Ministry of the Environment set up by the legal person for the verification of the principles, laboratory or sponsor of the study directly concerned by the specific control or audit of the study.

(4) In the event of non-compliance with the principles established at the time of periodic inspection or at the request of the certificate holder, the Ministry of the Environment may revoke the certificate by decision.

(5) The certificate expires

(a) death or declaration of death;

(b) the disappearance of a legal person; or

(c) a decision to revoke the certificate.

(6) The implementing act shall set out the scope of information on compliance with the principles to be provided for the entry and periodic review and audit of the study, the model of the certificate, the process of entry control, periodic checks and audits of the study and the details of the report on their progress.

Testing of the substance and mixture

§ 21

(1) Testing of hazardous properties of a substance or mixture shall be carried out for the purposes of this Act for the substance and mixture in the state in which it is produced or placed on the market.

(2) The person carrying out the test of the hazardous properties of the substance or mixture must confirm in writing that the tests have been carried out in accordance with the principles when submitting the results of such testing.

HLAVA IV

PROVISION OF INFORMATION

§ 22

Notification obligation

(1) The importer or downstream user (23), the first to place on the market of the European Union in the territory of the Czech Republic a mixture which has dangerous physicochemical properties or dangerous properties affecting health, is required to provide the Ministry of Health, through a portal managed by the European Chemicals Agency, with information on its effect on health to the extent and in the manner set out in Annex VIII, directly applicable European Union legislation on the classification, packaging and labelling of substances and mixtures (21).

(2) A distributor which places on the market in the territory of the Czech Republic a mixture which has dangerous physicochemical properties or dangerous properties affecting health shall, before the first placing on the market of that mixture, provide the Ministry of Health through a portal managed by the European Chemicals Agency with information on its effect on health to the extent and in the manner set out in Annex VIII, directly applicable European Union legislation on the classification, packaging and labelling of substances and mixtures (21), unless such information has been provided to the Ministry of Health pursuant to paragraph 1 or the distributor changes the designation of that mixture. The supplier may fulfil the obligation under the previous sentence as a distributor if they so agree; the responsibility for fulfilling this obligation remains with the distributor.

(3) The manufacturer who places a detergent on the market of the European Union within the territory of the Czech Republic shall, within 45 days of the date on which he first placed that detergent on the market, provide the Ministry of Health with the information contained in the data sheet in accordance with the directly applicable European Union law on detergenetech24) in electronic form.

(4) A distributor who places a detergent in the territory of the Czech Republic from another Member State of the European Union on the market shall, within 45 days of the date on which that detergent was first placed on the market, provide the Ministry of Health with the information published by the manufacturer in accordance with the directly applicable European Union regulation on detergenetech24) in electronic form.

(5) The importer, downstream user or distributor referred to in paragraphs 1 and 2 is required to update the information provided under paragraph 1 or 2 to the extent and in the manner set out in this Annex before the mixture is placed on the market, in accordance with Section 4.1 of Part B of Annex VIII. The manufacturer or distributor referred to in paragraphs 3 and 4 shall notify any change in the information provided to the Ministry of Health within 45 days of the change in the information.

(6) The implementing act shall specify the scope of the information required under paragraphs 3 and 4.

(7) The supplier of the article shall, before placing the article on the market, provide the information referred to in Article 33 (1) of the directly applicable European Union Regulation on the Registration, Evaluation, Authorisation and Restriction of Chemicals (29) to the database maintained by the European Chemicals Agency (30).

HLAVA V

PERFORMANCE OF STATE MANAGEMENT

§ 23

Government authorities

State administration in the field of the placing on the market, use and use of substances or substances contained in mixtures and articles under this Act

(a) Ministry of the Environment,

(b) Ministry of Health,

(c) Ministry of Industry and Trade,

(d) Ministry of Defence;

(e) Czech environmental inspection,

(f) regional health centres,

(g) customs offices,

(h) State Labour Inspection Office;

(i) Central control and testing institutes of agriculture.

§ 24

Ministry of Environment

(1) Ministry of the Environment

(a) is a central authority of the State in the field of environmental protection against the harmful effects of substances, mixtures or substances contained in mixtures and articles;

(b) is a central contact point in accordance with directly applicable European Union20), 21) for the purpose of providing advice to manufacturers, importers, downstream users and other interested parties on their obligations and responsibilities under these Regulations;

(c) exercise national supervision in the field of environmental protection against the harmful effects of substances, mixtures or substances contained in mixtures or articles manufactured, placed on the market or used;

(d) issue and revoke certificates of compliance pursuant to Articles 19 (1) and 20 (4);

(e) keep a list of the holders of compliance certificates and publish them in the Ministry of the Environment Bulletin;

(f) perform the function of competent authority in accordance with the provisions directly applicable to the European Union2) and represent the Czech Republic in the bodies of the European Chemicals Agency;

(g) allows exemptions under Article 2 (3) of Regulation (EC) No 1907 / 200620 of the European Parliament and of the Council or Article 1 (4) of Regulation (EC) No 1272 / 200821 of the European Parliament and of the Council),

(h) inform the public of the risks of substances in accordance with the directly applicable European Union Regulation (20).

(2) It provides the Ministry of Health with information on the granting of an exemption pursuant to Articles 14 (1) and 15 (1).

(3) The Ministry of the Environment provides the competent authorities of the European Union and the European Chemicals Agency with a report and an opinion within its scope, in accordance with the requirements of European Union regulations on the environmental protection sector against the harmful effects of substances or substances contained in mixtures and articles and mixtures.

(4) The Ministry of the Environment cooperates with the competent authorities of the European Union, the European Chemicals Agency and the competent authorities of the Member States of the European Union on the environmental protection sector against the harmful effects of substances or substances contained in mixtures and articles and mixtures.

(5) The Ministry of the Environment shall, within the scope of its competence as referred to in paragraph 1 (f), accept the notification referred to in Article 8 (3) of Regulation (EU) 2017 / 852 of the European Parliament and of the Council, assess its completeness and evaluate the information referred to in Article 8 (4) of this Regulation; In the framework of the evaluation, it shall seek the opinion of the Ministry of Health.

(6) If the Ministry of the Environment finds that the notification does not contain all the information referred to in Article 8 (3) of Regulation (EU) 2017 / 852 of the European Parliament and of the Council, or if additional information is requested by the Ministry of Health pursuant to Article 25 (5), it shall invite the notifier to complete the notification and shall set a reasonable time limit for it. Where the notifier fails to complete the notification within the time limit set, the information referred to in Article 8 (3) (a), (b) and (d) of Regulation (EU) 2017 / 852 of the European Parliament and of the Council shall be considered not to have been submitted.

(7) The Ministry of the Environment shall, within 30 days of the date of receipt of the opinion of the Ministry of Health, forward the notification to the European Commission if, on the basis of the evaluation carried out, it finds that the criteria referred to in the first subparagraph of Article 8 (6) of Regulation (EU) 2017 / 852 of the European Parliament and of the Council have been met. Otherwise, the Ministry of the Environment shall inform the notifier within the same time limit, stating the reasons for the non-compliance.

§ 25

Ministry of Health

(1) Ministry of Health

(a) is a central authority of the State on the public health sector against the harmful effects of substances, mixtures or substances contained in mixtures and articles;

(b) receive and collect information submitted pursuant to Articles 22 (1) to (5) and 45 of the directly applicable European Union Regulation on the classification, packaging and labelling of substances and mixtures (21) and allow remote access to them to the Toxicological Information Centre;

(c) represents the Czech Republic in the bodies of the European Chemicals Agency;

(d) inform the public, within its competence, of the risks of substances or substances contained in mixtures and articles dangerous to health.

(2) The Ministry of Health shall provide the competent authorities of the European Union and the competent authorities of the Member States of the European Union with reports and opinions in accordance with the requirements of European Union legislation on the protection of public health against the harmful effects of substances, mixtures or substances contained in mixtures and articles.

(3) The Ministry of Health is cooperating with the competent authorities of the European Union and the competent authorities of the Member States of the European Union on the section for the protection of public health against the harmful effects of substances, mixtures or substances contained in mixtures and articles.

(4) At the request of the Ministry of the Environment pursuant to Article 24 (5), the Ministry of Health gives an opinion on the notification under Article 8 (3) of Regulation (EU) 2017 / 852 of the European Parliament and of the Council. This opinion shall include an assessment as to whether the criteria set out in the first subparagraph of Article 8 (6) of Regulation (EU) 2017 / 852 of the European Parliament and of the Council are met in terms of the benefits of a new product with added mercury or a new manufacturing process for human health, the risks to human health and the existence of feasible technical alternatives that would provide a comparable benefit to human health. The deadline for issuing this opinion shall be 4 months and, in particularly difficult cases, 7 months from the date of receipt of the request from the Ministry of the Environment.

(5) If the Ministry of Health finds that it is necessary to request additional information from the notifier to carry out the assessment referred to in paragraph 4, it shall request the Ministry of the Environment to request it from the notifier. Pending the submission by the Ministry of Environment of supplementary information to the Ministry of Health, the deadline for the opinion referred to in paragraph 4 shall not run.

(6) The Ministry of Health issues a national plan pursuant to Article 10 (3) of Regulation (EU) 2017 / 852 of the European Parliament and of the Council.

§ 26

Ministry of Industry and Trade

(a) represents the Czech Republic in the bodies of the European Chemicals Agency;

(b) cooperate with the Ministry of the Environment in providing advice to manufacturers, importers, downstream users and other interested parties on their obligations and responsibilities under the directly applicable European Union regulations, 20), 21)

(c) inform the public of the risks of substances as referred to in Article 123 of the directly applicable European Union Regulation on the Registration, Evaluation, Authorisation and Restriction of Chemicals 20).

§ 26a

Ministry of Defence

(a) represents the Czech Republic in the institution of the European Defence Agency for the Coordination of the Implementation of the Code of Conduct for the Authorisation of Exemptions from the Regulation of the European Parliament and of the Council on the Registration, Evaluation, Authorisation and Restriction of Chemicals for the Protection of the State;

(b) cooperate with the Ministry of the Environment in providing advice to manufacturers and importers concerning their obligations and responsibilities under the directly applicable European Union legislation on classification, labelling and packaging of substances and mixtures (21); and

(c) issue, at the request of the Ministry of the Environment, a binding opinion for the granting of a decision authorising an exemption pursuant to Article 2 (3) of Regulation (EC) No 1907 / 200620 of the European Parliament and of the Council, within 20 days of the date of receipt of the application; This binding opinion shall include an assessment as to whether the requested exemption is necessary for the purpose of ensuring State defence.

§ 27

Czech Environmental Inspection

(a) checks that manufacturers, importers, downstream users, distributors and suppliers of articles comply with the provisions of this Act, the legislation issued for its implementation, the directly applicable European Union2 provisions) and administrative decisions under this Act;

(b) impose fines for infringement of obligations under this law, the legislation issued for its implementation, the provisions directly applicable to the European Union2) and decisions of the administrative authorities under this law.

§ 28

Regional Sanitation Station

(a) checks that manufacturers, importers, downstream users, distributors and suppliers of articles comply with the provisions of this Act, the legislation issued for its implementation, the directly applicable European Union2 provisions) and decisions of administrative bodies under this Act, in terms of health protection;

(b) checks compliance with the provisions of this Act, the legislation issued for its implementation, the directly applicable European Union2 provisions) and the decisions of administrative authorities issued pursuant to this Act, provided that they regulate the content of substances in articles intended to come into contact with food, toys, cosmetic products, products for children under the age of 3 years and products intended to come into direct contact with drinking, hot or rough water when they are taken, collected, transported, modified, divorced, collected, measured supply and other similar purposes;

(c) impose fines for infringement of obligations under this Act, the legislation issued for its implementation, the provisions directly applicable to the European Union2) and decisions of administrative authorities under this Act.

§ 29

State Labour Inspection Office

(a) checks that manufacturers, importers, downstream users, distributors and suppliers of articles comply with the provisions of this Act, the legislation issued for its implementation, the directly applicable European Union2 provisions) and decisions of administrative bodies under this Act, in terms of occupational safety,

(b) impose fines for infringement of obligations under this law, the legislation issued for its implementation, the provisions directly applicable to the European Union2) and decisions of the administrative authorities under this law.

§ 30

Customs office

(a) keeps records of all substances and mixtures exported from the Czech Republic and imported into the Czech Republic. This register will allow employees of the Ministry of the Environment, the Ministry of Health, the Czech Environmental Inspection, the Central Audit and Examination Institute of Agricultural and Regional Health Stations to view, extract or copy,

(b) controls the compliance of exporters and importers with the provisions of this Act, the legislation adopted for its implementation, the directly applicable provisions of the European Union2) and administrative decisions under this Act;

(c) impose fines for infringement of obligations under this Act, the legislation issued for its implementation, the provisions directly applicable to the European Union2) and decisions of administrative authorities under this Act.

§ 31

Central control and testing institute of agriculture

(a) checks compliance by suppliers of substances and mixtures with the provisions of this Act, the legislation adopted to implement it, the provisions directly applicable to the European Union and the decisions of the administrative authorities under this Act as regards the classification, packaging and labelling of plant protection products;

(b) impose fines for infringement of obligations under this Act, legislation issued for its implementation, directly applicable European Union2 provisions) and administrative decisions under this Act and give the Ministry of the Environment incentives to exercise state control against harmful effects produced, placed on the market or used plant protection products or other plant protection products.

HLAVA VI

CORRECTION AND TRANSFER MEASURES

§ 33

Corrective measures

(1) The competent administrative authorities under Article 23 (e) to (i) are entitled to order:

(a) a person who has placed a substance or mixture on the market contrary to the classification, packaging or labelling requirements laid down directly by the applicable European Union Regulation on classification, packaging and labelling (21) in order to suspend their further placing on the market until such requirements are complied with,

(b) a person who has placed a substance or substance in a mixture or article on the market without complying with the obligation to register under the directly applicable European Union Regulation on the Registration, Evaluation, Authorisation and Restriction of Chemicals (20), its withdrawal from the market;

(c) a person who has infringed the prohibition or restriction on the placing on the market of a substance on its own or contained in a mixture or article referred to in Titles VII and VIII of the directly applicable European Union Regulation on the Registration, Evaluation, Authorisation and Restriction of Chemicals (20), its withdrawal from the market;

(d) to eliminate the unlawful situation in the marketing of substances, mixtures or articles at the expense of their owner or holder, if the owner is not aware, if there is a risk of harm to human health, the environment or if it has already occurred;

(e) to eliminate the unlawful situation in the field of the import and export of substances, mixtures or articles of the disposal of a dangerous substance, mixture or article at the expense of their owner or holder, if the owner is not aware, if there is a risk of harm to human health or a threat to human life, the environment or if it has already occurred;

(f) to eliminate the unlawful situation in the field of the placing on the market of plant protection products or other plant protection products by the disposal of a dangerous plant protection product or of another plant protection product or of a parallel plant protection product at the expense of their owner or holder, if the owner is not aware, if there is a risk of harm to human or animal health or damage to the environment or if it has already occurred;

(g) a person who has placed on the market a surfactant or detergent containing a surfactant that does not meet the biodegradability criteria laid down by the directly applicable European Union detergenation28), their withdrawal from the market,

(h) to a person who has placed on the market a detergent which does not comply with the restrictions on the content of phosphates and other phosphorus compounds provided for in the directly applicable European Union regulation on detergenitech28), its withdrawal from the market; or

(i) a person who, contrary to Regulation (EU) 2017 / 852 of the European Parliament and of the Council, has placed on the market a new mercury-added product, its withdrawal from the market.

(2) An appeal against a decision to withdraw a substance, mixture or article from the market or the disposal of a dangerous substance, mixture or article shall not have suspensory effect.

§ 34

Transfers of legal and business natural persons

(1) A person who carries out testing of the properties of substances or mixtures dangerous to health and the environment for the purposes of this Act shall commit an offence by:

(a) carry out testing of dangerous properties of a substance or mixture for the purposes of this Act and directly applicable European Union20), 21) without certification pursuant to Paragraph 18 (1); or

(b) in contravention of Paragraph 21 (2), it shall not confirm in writing that testing of the hazardous properties of the substance or mixture has been carried out in accordance with the principles.

(2) The manufacturer or importer commits an infringement by:

(a) produce or import a substance or substance in a mixture or article without registration or notification under the directly applicable European Union Regulation on the Registration, Evaluation, Authorisation and Restriction of Chemicals (20); or

(b) in contravention of the directly applicable European Union Regulation on classification, labelling and packaging of substances and mixtures (21), they shall not notify classification data.

(3) The manufacturer commits an offence by placing on the market in the Czech Republic, contrary to the directly applicable European Union regulation on detergenitech28

(a) a surfactant or detergent containing a surfactant that does not comply with the biodegradability criteria laid down by the directly applicable European Union detergento28); or

(b) consumer detergent or detergent intended for automatic dishwashers for consumers.

(4) The manufacturer, importer or downstream user commits an infringement by:

(a) in contravention of the directly applicable European Union Regulation on the Registration, Evaluation, Authorisation and Restriction of Chemicals (20), it shall place on the market or use a substance without authorisation;

(b) in contravention of the directly applicable European Union regulation on persistent organic pollutants (25), produce, place on the market or use a substance; or

(c) in contravention of the directly applicable European Union legislation on classification, labelling and packaging of substances and mixtures (21), it does not classify a substance or mixture before being placed on the market or classifies it differently than that provided for in this Regulation.

(5) The manufacturer, importer, downstream user or distributor commits an infringement by:

(a) in contravention of the directly applicable European Union Regulation on the Registration, Evaluation, Authorisation and Restriction of Chemicals (20), does not provide information in the supply chain;

(b) in contravention of Title VIII, the directly applicable European Union Regulation on the Registration, Evaluation, Authorisation and Restriction of Chemical Substances (20) shall be manufactured, placed on the market or used in a mixture or article;

(c) placing on the market a substance or mixture classified as dangerous without ensuring its labelling and packaging in accordance with the directly applicable European Union Regulation on classification, labelling and packaging of substances and mixtures (21);

(d) in contravention of the directly applicable European Union Regulation on classification, labelling and packaging of substances and mixtures (21), does not retain evidence of compliance with the classification and labelling requirements of the substance or mixture for the period during which the substance or mixture is placed on the market and for a period of 10 years after the last placing on the market or does not provide it to the competent administrative authorities on request;

(e) in contravention of the directly applicable European Union regulation on classification, labelling and packaging of substances and mixtures (21), it shall not indicate the relevant hazard classes or categories in the supply of a dangerous substance or hazard information in the supply of a mixture which allows the conclusion of a sales contract without knowledge of the information on the label or packaging of the substance or mixture;

(f) in contravention of the directly applicable European Union Regulation on the Registration, Evaluation, Authorisation and Restriction of Chemicals (20), it shall not retain all the information required for the performance of its duties for as long as the substance or mixture is placed on the market and for a period of 10 years from the last placing on the market.

(6) The exporter or importer shall commit an offence by:

(a) in contravention of the directly applicable European Union Regulation on the export and import of dangerous chemical substances (26), imports or exports of a substance; or

(b) in contravention of the directly applicable European Union provisions on the export and import of hazardous chemical substances (26), the Ministry of the Environment shall not provide information on imports and exports.

(7) The exporter shall commit an offence by exporting mercury, its compounds or mixtures or by exporting mercury-added products in breach of Regulation (EU) 2017 / 852 of the European Parliament and of the Council.

(8) The importer shall commit an offence by importing mercury, its compounds or mixtures or by importing mercury-added products in breach of Regulation (EU) 2017 / 852 of the European Parliament and of the Council.

(9) A person commits an offence by violating Regulation (EU) 2017 / 852 of the European Parliament and of the Council

(a) produce a mercury-added product;

(b) use mercury or its compounds in the manufacturing process or the new manufacturing process;

(c) produce or market a new mercury-added product; or

(d) use free-packed mercury.

(10) A downstream user commits an infringement by violating the directly applicable European Union Regulation on the Registration, Evaluation, Authorisation and Restriction of Chemicals (20)

(a) not produce a chemical safety report or provide the European Chemicals Agency with the information specified; or

Citation	Act No. 350 / 2011 Coll., on Chemicals and Chemical Mixtures and on the Amendment of Certain Laws (Chemical Act)
Regulation Type	Law
Author	-
Collection	Code of Laws

Date of Promulgation	29.11.2011
Effective from	01.01.2012
Effective until	-
Status	Valid

Act No. 350 / 2011 Coll.

Law on chemicals and chemical mixtures and on the modification of certain laws (chemical law)

Contents