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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/ECRegistration – REACH
- Recitals
TITLE I — GENERAL ISSUES- 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
- CHAPTER 3 — Obligation to register and information requirements for certain types of isolated intermediates
- CHAPTER 4 — Common provisions for all registrations
- CHAPTER 5 — Transitional provisions applicable to phase-in substances and notified substances
- TITLE III — DATA SHARING AND AVOIDANCE OF UNNECESSARY TESTING
- 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
- TITLE VI — EVALUATION
- CHAPTER 1 — Dossier evaluation
- CHAPTER 2 — Substance evaluation
- CHAPTER 3 — Evaluation of 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
- TITLE VIII — RESTRICTIONS ON THE MANUFACTURING, PLACING ON THE MARKET AND USE OF CERTAIN DANGEROUS SUBSTANCES, MIXTURES AND ARTICLES
- CHAPTER 1 — General issues
- 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
- 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
- TITLE XIII — COMPETENT AUTHORITIES
- TITLE XIV — ENFORCEMENT
- 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
- Final
- LIST OF ANNEXES
- ANNEX I — GENERAL PROVISIONS FOR ASSESSING SUBSTANCES AND PREPARING CHEMICAL SAFETY REPORTS
- ANNEX II — REQUIREMENTS FOR THE COMPILATION OF SAFETY DATA SHEETS
- ANNEX III — CRITERIA FOR SUBSTANCES REGISTERED IN QUANTITIES BETWEEN 1 AND 10 TONNES
- ANNEX IV
- ANNEX V — EXEMPTIONS FROM THE OBLIGATION TO REGISTER IN ACCORDANCE WITH ARTICLE 2(7)(b)
- ANNEX VI — INFORMATION REQUIREMENTS REFERRED TO IN ARTICLE 10
- ANNEX VII — STANDARD INFORMATION REQUIREMENTS FOR SUBSTANCES MANUFACTURED OR IMPORTED IN QUANTITIES OF ONE TONNE OR MORE(1)
- ANNEX VIII — STANDARD INFORMATION REQUIREMENTS FOR SUBSTANCES MANUFACTURED OR IMPORTED IN QUANTITIES OF 10 TONNES OR MORE(1)
- ANNEX IX — STANDARD INFORMATION REQUIREMENTS FOR SUBSTANCES MANUFACTURED OR IMPORTED IN QUANTITIES OF 100 TONNES OR MORE(1)
- ANNEX X — STANDARD INFORMATION REQUIREMENTS FOR SUBSTANCES MANUFACTURED OR IMPORTED IN QUANTITIES OF 1000 TONNES OR MORE(1)
- ANNEX XI — GENERAL RULES FOR ADAPTATION OF THE STANDARD TESTING REGIME SET OUT IN ANNEXES VII TO X
- ANNEX XII — GENERAL PROVISIONS FOR DOWNSTREAM USERS TO ASSESS SUBSTANCES AND PREPARE CHEMICAL SAFETY REPORTS
- ANNEX XIII — CRITERIA FOR THE IDENTIFICATION OF PERSISTENT, BIOACCUMULATIVE AND TOXIC SUBSTANCES, AND VERY PERSISTENT AND VERY BIOACCUMULATIVE SUBSTANCES
- ANNEX XIV — LIST OF SUBSTANCES SUBJECT TO AUTHORISATION
- ANNEX XV — DOSSIERS
- ANNEX XVI — SOCIO-ECONOMIC ANALYSIS
- ANNEX XVII — RESTRICTIONS ON THE MANUFACTURE, PLACING ON THE MARKET AND USE OF CERTAIN DANGEROUS SUBSTANCES, MIXTURES AND ARTICLES