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Regulation (EC) No 1907/2006 of the European Parliament and of the Council of 18 December 2006 concerning the Registration, Evaluation, Authorisation and Restriction of Chemicals (REACH), establishing a European Chemicals Agency, amending Directive 1999/45/EC and repealing Council Regulation (EEC) No 793/93 and Commission Regulation (EC) No 1488/94 as well as Council Directive 76/769/EEC and Commission Directives 91/155/EEC, 93/67/EEC, 93/105/EC and 2000/21/EC (Text with EEA relevance)Text with EEA relevance

Regulation (EC) No 1907/2006 of the European Parliament and of the Council of 18 December 2006 concerning the Registration, Evaluation, Authorisation and Restriction of Chemicals (REACH), establishing a European Chemicals Agency, amending Directive 1999/45/EC and repealing Council Regulation (EEC) No 793/93 and Commission Regulation (EC) No 1488/94 as well as Council Directive 76/769/EEC and Commission Directives 91/155/EEC, 93/67/EEC, 93/105/EC and 2000/21/EC (Text with EEA relevance)Text with EEA relevance

TITLE I GENERAL ISSUES

CHAPTER 1 Aim, scope and application

Article 1 Aim and scope

1.

The purpose of this Regulation is to ensure a high level of protection of human health and the environment, including the promotion of alternative methods for assessment of hazards of substances, as well as the free circulation of substances on the internal market while enhancing competitiveness and innovation.

2.

This Regulation lays down provisions on substances and mixtures within the meaning of Article 3. These provisions shall apply to the manufacture, placing on the market or use of such substances on their own, in mixtures or in articles and to the placing on the market of mixtures.

3.

This Regulation is based on the principle that it is for manufacturers, importers and downstream users to ensure that they manufacture, place on the market or use such substances that do not adversely affect human health or the environment. Its provisions are underpinned by the precautionary principle.

Article 2 Application

1.

This Regulation shall not apply to:

  1. radioactive substances within the scope of Council Directive 96/29/Euratom of 13 May 1996 laying down basic safety standards for the protection of the health of workers and the general public against the dangers arising from ionising radiation(1);

  2. substances, on their own, in a mixture or in an article, which are subject to customs supervision, provided that they do not undergo any treatment or processing, and which are in temporary storage, or in a free zone or free warehouse with a view to re-exportation, or in transit;

  3. non-isolated intermediates;

  4. the carriage of dangerous substances and dangerous substances in dangerous mixtures by rail, road, inland waterway, sea or air.

2.

Waste as defined in Directive 2006/12/EC of the European Parliament and of the Council(2) is not a substance, mixture or article within the meaning of Article 3 of this Regulation.

3.

Member States may allow for exemptions from this Regulation in specific cases for certain substances, on their own, in a mixture or in an article, where necessary in the interests of defence.

4.

This Regulation shall apply without prejudice to:

  1. Community workplace and environmental legislation, including Council Directive 89/391/EEC of 12 June 1989 on the introduction of measures to encourage improvements in the safety and health of workers at work(3), Council Directive 96/61/EC of 24 September 1996 concerning integrated pollution prevention and control(4); Directive 98/24/EC, Directive 2000/60/EC of the European Parliament and of the Council of 23 October 2000 establishing a framework for Community action in the field of water policy(5) and Directive 2004/37/EC;

  2. Directive 76/768/EEC as regards testing involving vertebrate animals within the scope of that Directive.

5.

The provisions of Titles II, V, VI and VII shall not apply to the extent that a substance is used:

  1. in medicinal products for human or veterinary use within the scope of Regulation (EC) No 726/2004, Directive 2001/82/EC of the European Parliament and of the Council of 6 November 2001 on the Community code relating to veterinary medicinal products(6) and Directive 2001/83/EC of the European Parliament and of the Council of 6 November 2001 on the Community code relating to medicinal products for human use(7);

  2. in food or feedingstuffs in accordance with Regulation (EC) No 178/2002 including use:

    1. as a food additive in foodstuffs within the scope of Council Directive 89/107/EEC of 21 December 1988 on the approximation of the laws of the Member States concerning food additives authorised for use in foodstuffs intended for human consumption(8);

    2. as a flavouring in foodstuffs within the scope of Council Directive 88/388/EEC of 22 June 1988 on the approximation of the laws of the Member States relating to flavourings for use in foodstuffs and to source materials for their production(9) and Commission Decision 1999/217/EC of 23 February 1999 adopting a register of flavouring substances used in or on foodstuffs drawn up in application of Regulation (EC) No 2232/96 of the European Parliament and of the Council(10);

    3. as an additive in feedingstuffs within the scope of Regulation (EC) No 1831/2003 of the European Parliament and of the Council of 22 September 2003 on additives for use in animal nutrition(11);

    4. in animal nutrition within the scope of Council Directive 82/471/EEC of 30 June 1982 concerning certain products used in animal nutrition(12).

6.

The provisions of Title IV shall not apply to the following mixtures in the finished state, intended for the final user:

  1. medicinal products for human or veterinary use, within the scope of Regulation (EC) No 726/2004 and Directive 2001/82/EC and as defined in Directive 2001/83/EC;

  2. cosmetic products as defined in Directive 76/768/EEC;

  3. medical devices which are invasive or used in direct physical contact with the human body in so far as Community measures lay down provisions for the classification and labelling of dangerous substances and mixtures which ensure the same level of information provision and protection as Directive 1999/45/EC;

  4. food or feedingstuffs in accordance with Regulation (EC) No 178/2002 including use:

    1. as a food additive in foodstuffs within the scope of Directive 89/107/EEC;

    2. as a flavouring in foodstuffs within the scope of Directive 88/388/EEC and Decision 1999/217/EC;

    3. as an additive in feedingstuffs within the scope of Regulation (EC) No 1831/2003;

    4. in animal nutrition within the scope of Directive 82/471/EEC.

7.

The following shall be exempted from Titles II, V and VI:

  1. substances included in Annex IV, as sufficient information is known about these substances that they are considered to cause minimum risk because of their intrinsic properties;

  2. substances covered by Annex V, as registration is deemed inappropriate or unnecessary for these substances and their exemption from these Titles does not prejudice the objectives of this Regulation;

  3. substances on their own or in mixtures, registered in accordance with Title II, exported from the Community by an actor in the supply chain and re-imported into the Community by the same or another actor in the same supply chain who shows that:

    1. the substance being re-imported is the same as the exported substance;

    2. he has been provided with the information in accordance with Articles 31 or 32 relating to the exported substance;

  4. substances, on their own, in mixtures or in articles, which have been registered in accordance with Title II and which are recovered in the Community if:

    1. the substance that results from the recovery process is the same as the substance that has been registered in accordance with Title II; and

    2. the information required by Articles 31 or 32 relating to the substance that has been registered in accordance with Title II is available to the establishment undertaking the recovery.

8.

On-site isolated intermediates and transported isolated intermediates shall be exempted from:

  1. Chapter 1 of Title II, with the exception of Articles 8 and 9; and

  2. Title VII.

9.

The provisions of Titles II and VI shall not apply to polymers.

CHAPTER 2 Definitions and general provision

Article 3 Definitions

Article 4 General provision

TITLE II REGISTRATION OF SUBSTANCES

CHAPTER 1 General obligation to register and information requirements

Article 5 No data, no market

Article 6 General obligation to register substances on their own or in mixtures

Article 7 Registration and notification of substances in articles

Article 8 Only representative of a non-Community manufacturer

Article 9 Exemption from the general obligation to register for product and process orientated research and development (PPORD)

Article 10 Information to be submitted for general registration purposes

Article 11 Joint submission of data by multiple registrants

Article 12 Information to be submitted depending on tonnage

Article 13 General requirements for generation of information on intrinsic properties of substances

Article 14 Chemical safety report and duty to apply and recommend risk reduction measures

CHAPTER 2 Substances regarded as being registered

Article 15 Substances in plant protection and biocidal products

Article 16 Duties of the Commission, the Agency and registrants of substances regarded as being registered

CHAPTER 3 Obligation to register and information requirements for certain types of isolated intermediates

Article 17 Registration of on-site isolated intermediates

Article 18 Registration of transported isolated intermediates

Article 19 Joint submission of data on isolated intermediates by multiple registrants

CHAPTER 4 Common provisions for all registrations

Article 20 Duties of the Agency

Article 21 Manufacturing and import of substances

Article 22 Further duties of registrants

CHAPTER 5 Transitional provisions applicable to phase-in substances and notified substances

Article 23 Specific provisions for phase-in substances

Article 24 Notified substances

TITLE III DATA SHARING AND AVOIDANCE OF UNNECESSARY TESTING

CHAPTER 1 Objectives and general rules

Article 25 Objectives and general rules

CHAPTER 2 Rules for non-phase-in substances and registrants of phase-in substances who have not pre-registered

Article 26 Duty to inquire prior to registration

Article 27 Sharing of existing data in the case of registered substances

CHAPTER 3 Rules for phase-in-substances

Article 28 Duty to pre-register for phase-in substances

Article 29 Substance Information Exchange Forums

Article 30 Sharing of data involving tests

TITLE IV INFORMATION IN THE SUPPLY CHAIN

Article 31 Requirements for safety data sheets

Article 32 Duty to communicate information down the supply chain for substances on their own or in mixtures for which a safety data sheet is not required

Article 33 Duty to communicate information on substances in articles

Article 34 Duty to communicate information on substances and mixtures up the supply chain

Article 35 Access to information for workers

Article 36 Obligation to keep information

TITLE V DOWNSTREAM USERS

Article 37 Downstream user chemical safety assessments and duty to identify, apply and recommend risk reduction measures

Article 38 Obligation for downstream users to report information

Article 39 Application of downstream user obligations

TITLE VI EVALUATION

CHAPTER 1 Dossier evaluation

Article 40 Examination of testing proposals

Article 41 Compliance check of registrations

Article 42 Check of information submitted and follow-up to dossier evaluation

Article 43 Procedure and time periods for examination of testing proposals

CHAPTER 2 Substance evaluation

Article 44 Criteria for substance evaluation

Article 45 Competent authority

Article 46 Requests for further information and check of information submitted

Article 47 Coherence with other activities

Article 48 Follow-up to substance evaluation

CHAPTER 3 Evaluation of intermediates

Article 49 Further information on on-site isolated intermediates

CHAPTER 4 Common provisions

Article 50 Registrants' and downstream users' rights

Article 51 Adoption of decisions under dossier evaluation

Article 52 Adoption of decisions under substance evaluation

Article 53 Cost sharing for tests without an agreement between registrants and/or downstream users

Article 54 Publication of information on evaluation

TITLE VII AUTHORISATION

CHAPTER 1 Authorisation requirement

Article 55 Aim of authorisation and considerations for substitution

Article 56 General provisions

Article 57 Substances to be included in Annex XIV

Article 58 Inclusion of substances in Annex XIV

Article 59 Identification of substances referred to in Article 57

CHAPTER 2 Granting of authorisations

Article 60 Granting of authorisations

Article 61 Review of authorisations

Article 62 Applications for authorisations

Article 63 Subsequent applications for authorisation

Article 64 Procedure for authorisation decisions

CHAPTER 3 Authorisations in the supply chain

Article 65 Obligation of holders of authorisations

Article 66 Downstream users

TITLE VIII RESTRICTIONS ON THE MANUFACTURING, PLACING ON THE MARKET AND USE OF CERTAIN DANGEROUS SUBSTANCES, MIXTURES AND ARTICLES

CHAPTER 1 General issues

Article 67 General provisions

CHAPTER 2 Restrictions process

Article 68 Introducing new and amending current restrictions

Article 69 Preparation of a proposal

Article 70 Agency opinion: Committee for Risk Assessment

Article 71 Agency opinion: Committee for Socio-economic Analysis

Article 72 Submission of an opinion to the Commission

Article 73 Commission decision

TITLE IX FEES AND CHARGES

Article 74 Fees and charges

TITLE X AGENCY

Article 75 Establishment and review

Article 76 Composition

Article 77 Tasks

Article 78 Powers of the Management Board

Article 79 Composition of the Management Board

Article 80 Chairmanship of the Management Board

Article 81 Meetings of the Management Board

Article 82 Voting of the Management Board

Article 83 Duties and powers of the Executive Director

Article 84 Appointment of the Executive Director

Article 85 Establishment of the Committees

Article 86 Establishment of the Forum

Article 87 Rapporteurs of Committees and use of experts

Article 88 Qualification and interests

Article 89 Establishment of the Board of Appeal

Article 90 Members of the Board of Appeal

Article 91 Decisions subject to appeal

Article 92 Persons entitled to appeal, time-limits, fees and form

Article 93 Examination and decisions on appeal

Article 94 Actions before the Court of First Instance and the Court of Justice

Article 95 Conflicts of opinion with other bodies

Article 96 The budget of the Agency

Article 97 Implementation of the budget of the Agency

Article 98 Combating fraud

Article 99 Financial rules

Article 100 Legal personality of the Agency

Article 101 Liability of the Agency

Article 102 Privileges and immunities of the Agency

Article 103 Staff rules and regulations

Article 104 Languages

Article 105 Duty of confidentiality

Article 106 Participation of third countries

Article 107 Participation of international organisations

Article 108 Contacts with stakeholder organisations

Article 109 Rules on transparency

Article 110 Relations with relevant Community bodies

Article 111 Formats and software for submission of information to the Agency

TITLE XII INFORMATION

Article 117 Reporting

Article 118 Access to information

Article 119 Electronic public access

Article 120 Cooperation with third countries and international organisations

TITLE XIII COMPETENT AUTHORITIES

Article 121 Appointment

Article 122 Cooperation between competent authorities

Article 123 Communication to the public of information on risks of substances

Article 124 Other responsibilities

TITLE XIV ENFORCEMENT

Article 125 Tasks of the Member States

Article 126 Penalties for non-compliance

Article 127 Report

TITLE XV TRANSITIONAL AND FINAL PROVISIONS

Article 128 Free movement

Article 129 Safeguard clause

Article 130 Statement of reasons for decisions

Article 131 Amendments to the Annexes

Article 132 Implementing legislation

Article 133 Committee procedure

Article 134 Preparation of establishment of the Agency

Article 135 Transitional measures regarding notified substances

Article 136 Transitional measures regarding existing substances

Article 137 Transitional measures regarding restrictions

Article 138 Review

Article 139 Repeals

Article 140 Amendment of Directive 1999/45/EC

Article 141 Entry into force and application

LIST OF ANNEXES

ANNEX IGENERAL PROVISIONS FOR ASSESSING SUBSTANCES AND PREPARING CHEMICAL SAFETY REPORTS

ANNEX IIREQUIREMENTS FOR THE COMPILATION OF SAFETY DATA SHEETS

ANNEX IIICRITERIA FOR SUBSTANCES REGISTERED IN QUANTITIES BETWEEN 1 AND 10 TONNES

ANNEX IV

ANNEX V

ANNEX VIINFORMATION REQUIREMENTS REFERRED TO IN ARTICLE 10

ANNEX VIISTANDARD INFORMATION REQUIREMENTS FOR SUBSTANCES MANUFACTURED OR IMPORTED IN QUANTITIES OF ONE TONNE OR MORE(59)

ANNEX VIIISTANDARD INFORMATION REQUIREMENTS FOR SUBSTANCES MANUFACTURED OR IMPORTED IN QUANTITIES OF 10 TONNES OR MORE(61)

ANNEX IXSTANDARD INFORMATION REQUIREMENTS FOR SUBSTANCES MANUFACTURED OR IMPORTED IN QUANTITIES OF 100 TONNES OR MORE(63)

ANNEX XSTANDARD INFORMATION REQUIREMENTS FOR SUBSTANCES MANUFACTURED OR IMPORTED IN QUANTITIES OF 1 000 TONNES OR MORE(65)

ANNEX XIGENERAL RULES FOR ADAPTATION OF THE STANDARD TESTING REGIME SET OUT IN ANNEXES VII TO X

ANNEX XIIGENERAL PROVISIONS FOR DOWNSTREAM USERS TO ASSESS SUBSTANCES AND PREPARE CHEMICAL SAFETY REPORTS

ANNEX XIII

ANNEX XIVLIST OF SUBSTANCES SUBJECT TO AUTHORISATION

ANNEX XVDOSSIERS

ANNEX XVISOCIO-ECONOMIC ANALYSIS

ANNEX XVIIRESTRICTIONS ON THE MANUFACTURE, PLACING ON THE MARKET AND USE OF CERTAIN DANGEROUS SUBSTANCES, MIXTURES AND ARTICLES

Appendices 1 to 6

Appendix 1Entry 28 – Carcinogens: Category 1A

Appendix 2Entry 28 – Carcinogens: Category 1 B

Appendix 3Entry 29 – Germ cell mutagens: Category 1 A

Appendix 4Entry 29 – Germ cell mutagens: Category 1 B

Appendix 5Entry 30 – Reproductive toxicants: Category 1 A

Appendix 6Entry 30 – Reproductive toxicants: Category 1 B

Appendix 7Special provisions on the labelling of articles containing asbestos

Appendix 8Entry 43 — Azocolourants — List of aromatic amines

Appendix 9Entry 43 — Azocolourants — List of azodyes

Appendix 10

Appendix 11

Appendix 12

Appendix 13