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Commission
| Page | Keyword count |
| Preamble | 4 |
| TITLE I: GENERAL ISSUES | |
| CHAPTER 1: Aim, scope and application | |
| Article 2: Application | 1 |
| CHAPTER 2: Definitions and general provision | |
| Article 3: Definitions | 1 |
| TITLE II: REGISTRATION OF SUBSTANCES | |
| CHAPTER 1: General obligation to register and information requirements | |
| Article 13: General requirements for generation of information on intrinsic properties of substances | 7 |
| CHAPTER 2: Substances regarded as being registered | 1 |
| Article 15: Substances in plant protection and biocidal products | 6 |
| Article 16: Duties of the Commission, the Agency and registrants of substances regarded as being registered | 2 |
| TITLE VI: EVALUATION | |
| CHAPTER 1: Dossier evaluation | |
| Article 41: Compliance check of registrations | 1 |
| Article 42: Check of information submitted and follow-up to dossier evaluation | 1 |
| CHAPTER 2: Substance evaluation | |
| Article 45: Competent authority | 1 |
| Article 48: Follow-up to substance evaluation | 1 |
| CHAPTER 4: Common provisions | |
| Article 51: Adoption of decisions under dossier evaluation | 1 |
| TITLE VII: AUTHORISATION | |
| CHAPTER 1: Authorisation requirement | |
| Article 58: Inclusion of substances in Annex XIV | 1 |
| Article 59: Identification of substances referred to in Article 57 | 2 |
| CHAPTER 2: Granting of authorisations | |
| Article 60: Granting of authorisations | 4 |
| Article 61: Review of authorisations | 6 |
| Article 64: Procedure for authorisation decisions | 4 |
| 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 | 1 |
| CHAPTER 2: Restrictions process | 2 |
| Article 68: Introducing new and amending current restrictions | 1 |
| Article 69: Preparation of a proposal | 3 |
| Article 70: Agency opinion: Committee for Risk Assessment | 1 |
| Article 72: Submission of an opinion to the Commission | 4 |
| Article 73: Commission decision | 4 |
| TITLE IX: FEES AND CHARGES | |
| Article 74: Fees and charges | 1 |
| TITLE X: AGENCY | |
| Article 77: Tasks | 1 |
| Article 79: Composition of the Management Board | 2 |
| Article 83: Duties and powers of the Executive Director | 3 |
| Article 84: Appointment of the Executive Director | 1 |
| Article 85: Establishment of the Committees | 1 |
| Article 86: Establishment of the Forum | 1 |
| Article 89: Establishment of the Board of Appeal | 3 |
| Article 90: Members of the Board of Appeal | 1 |
| Article 93: Examination and decisions on appeal | 1 |
| Article 95: Conflicts of opinion with other bodies | 1 |
| Article 96: The budget of the Agency | 5 |
| Article 97: Implementation of the budget of the Agency | 4 |
| Article 99: Financial rules | 2 |
| Article 103: Staff rules and regulations | 2 |
| Article 108: Contacts with stakeholder organisations | 1 |
| Article 109: Rules on transparency | 1 |
| Article 110: Relations with relevant Community bodies | 2 |
| TITLE XII: INFORMATION | |
| Article 117: Reporting | 5 |
| TITLE XIII: COMPETENT AUTHORITIES | |
| Article 121: Appointment | 1 |
| TITLE XIV: ENFORCEMENT | |
| Article 126: Penalties for non-compliance | 1 |
| Article 127: Report | 1 |
| TITLE XV: TRANSITIONAL AND FINAL PROVISIONS | |
| Article 129: Safeguard clause | 4 |
| Article 130: Statement of reasons for decisions | 1 |
| Article 133: Committee procedure | 1 |
| Article 134: Preparation of establishment of the Agency | 2 |
| Article 136: Transitional measures regarding existing substances | 4 |
| Article 137: Transitional measures regarding restrictions | 3 |
| Article 138: Review | 15 |
| ANNEX I: GENERAL PROVISIONS FOR ASSESSING SUBSTANCES AND PREPARING CHEMICAL SAFETY REPORTS | |
| 1.: HUMAN HEALTH HAZARD ASSESSMENT | |
| 1.1.: Step 1: Evaluation of non-human information | 1 |
| ANNEX II: REQUIREMENTS FOR THE COMPILATION OF SAFETY DATA SHEETS | |
| 8.: SECTION 8: Exposure controls/personal protection | |
| 8.1.: Control parameters | 1 |
| ANNEX IX: STANDARD INFORMATION REQUIREMENTS FOR SUBSTANCES MANUFACTURED OR IMPORTED IN QUANTITIES OF 100 TONNES OR MORE | |
| 8.: TOXICOLOGICAL INFORMATION | 2 |
| ANNEX X: STANDARD INFORMATION REQUIREMENTS FOR SUBSTANCES MANUFACTURED OR IMPORTED IN QUANTITIES OF 1 000 TONNES OR MORE | |
| 8.: TOXICOLOGICAL INFORMATION | 1 |
| ANNEX XI: GENERAL RULES FOR ADAPTATION OF THE STANDARD TESTING REGIME SET OUT IN ANNEXES VII TO X | |
| 1.: TESTING DOES NOT APPEAR SCIENTIFICALLY NECESSARY | |
| 1.2.: Weight of evidence | 1 |
| 1.3.: Qualitative or Quantitative structure-activity relationship ((Q)SAR) | 1 |
| ANNEX XVII: RESTRICTIONS ON THE MANUFACTURE, PLACING ON THE MARKET AND USE OF CERTAIN DANGEROUS SUBSTANCES, MIXTURES AND ARTICLES | 14 |
| Appendix 11 | 15 |