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| Page | Keyword count |
| TITLE I: GENERAL ISSUES | |
| CHAPTER 1: Aim, scope and application | |
| Article 1: Aim and scope | 2 |
| Article 2: Application | 8 |
| CHAPTER 2: Definitions and general provision | |
| Article 3: Definitions | 8 |
| TITLE II: REGISTRATION OF SUBSTANCES | |
| CHAPTER 1: General obligation to register and information requirements | |
| Article 7: Registration and notification of substances in articles | 3 |
| Article 9: Exemption from the general obligation to register for product and process orientated research and development (PPORD) | 1 |
| Article 10: Information to be submitted for general registration purposes | 3 |
| Article 13: General requirements for generation of information on intrinsic properties of substances | 1 |
| Article 14: Chemical safety report and duty to apply and recommend risk reduction measures | 2 |
| CHAPTER 2: Substances regarded as being registered | |
| Article 15: Substances in plant protection and biocidal products | 4 |
| TITLE III: DATA SHARING AND AVOIDANCE OF UNNECESSARY TESTING | |
| 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 | 1 |
| CHAPTER 3: Rules for phase-in-substances | |
| Article 28: Duty to pre-register for phase-in substances | 1 |
| TITLE IV: INFORMATION IN THE SUPPLY CHAIN | |
| Article 31: Requirements for safety data sheets | 3 |
| Article 35: Access to information for workers | 1 |
| TITLE V: DOWNSTREAM USERS | |
| Article 37: Downstream user chemical safety assessments and duty to identify, apply and recommend risk reduction measures | 9 |
| Article 38: Obligation for downstream users to report information | 2 |
| TITLE VI: EVALUATION | |
| CHAPTER 1: Dossier evaluation | |
| Article 42: Check of information submitted and follow-up to dossier evaluation | 2 |
| CHAPTER 2: Substance evaluation | |
| Article 44: Criteria for substance evaluation | 1 |
| Article 48: Follow-up to substance evaluation | 2 |
| CHAPTER 3: Evaluation of intermediates | |
| Article 49: Further information on on-site isolated intermediates | 2 |
| CHAPTER 4: Common provisions | |
| Article 50: Registrants' and downstream users' rights | 3 |
| TITLE VII: AUTHORISATION | |
| CHAPTER 1: Authorisation requirement | |
| Article 56: General provisions | 12 |
| Article 58: Inclusion of substances in Annex XIV | 5 |
| CHAPTER 2: Granting of authorisations | |
| Article 60: Granting of authorisations | 6 |
| Article 61: Review of authorisations | 4 |
| Article 62: Applications for authorisations | 5 |
| Article 63: Subsequent applications for authorisation | 2 |
| Article 64: Procedure for authorisation decisions | 2 |
| 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 | 3 |
| CHAPTER 2: Restrictions process | |
| Article 68: Introducing new and amending current restrictions | 3 |
| Article 69: Preparation of a proposal | 3 |
| TITLE X: AGENCY | 1 |
| Article 77: Tasks | 1 |
| Article 83: Duties and powers of the Executive Director | 1 |
| Article 85: Establishment of the Committees | 1 |
| Article 87: Rapporteurs of Committees and use of experts | 2 |
| Article 111: Formats and software for submission of information to the Agency | 1 |
| TITLE XII: INFORMATION | |
| Article 117: Reporting | 1 |
| Article 118: Access to information | 2 |
| TITLE XV: TRANSITIONAL AND FINAL PROVISIONS | |
| Article 128: Free movement | 2 |
| Article 129: Safeguard clause | 1 |
| ANNEX I: GENERAL PROVISIONS FOR ASSESSING SUBSTANCES AND PREPARING CHEMICAL SAFETY REPORTS | |
| 0.: INTRODUCTION | 3 |
| 0.6.: Steps of a chemical safety assessment | 5 |
| 5.: EXPOSURE ASSESSMENT | |
| 5.0.: Introduction | 1 |
| 5.1.: Step 1: Development of exposure scenarios | 2 |
| 5.2.: Step 2: Exposure Estimation | 1 |
| 6.: RISK CHARACTERISATION | 1 |
| ANNEX II: REQUIREMENTS FOR THE COMPILATION OF SAFETY DATA SHEETS | |
| 0.2.: General requirements for compiling a safety data sheet | 1 |
| 0.5.: Other information requirements | 1 |
| 3.: SECTION 3: Composition/information on ingredients | |
| 3.2.: Mixtures | 1 |
| 4.: SECTION 4: First aid measures | 1 |
| 6.: SECTION 6: Accidental release measures | |
| 6.3.: Methods and material for containment and cleaning up | 2 |
| 7.: SECTION 7: Handling and storage | |
| 7.1.: Precautions for safe handling | 1 |
| 7.2.: Conditions for safe storage, including any incompatibilities | 1 |
| 8.: SECTION 8: Exposure controls/personal protection | |
| 8.2.: Exposure controls | |
| 8.2.2.: Individual protection measures, such as personal protective equipment | 1 |
| 10.: SECTION 10: Stability and reactivity | |
| 10.1.: Reactivity | 1 |
| 10.6.: Hazardous decomposition products | 1 |
| 11.: SECTION 11: Toxicological information | 1 |
| ANNEX VI: INFORMATION REQUIREMENTS REFERRED TO IN ARTICLE 10 | |
| guidance note on fulfilling the requirements of annexes vi to xi: GUIDANCE NOTE ON FULFILLING THE REQUIREMENTS OF ANNEXES VI TO XI | 1 |
| STEP 1: GATHER AND SHARE EXISTING INFORMATION | 1 |
| STEP 2: CONSIDER INFORMATION NEEDS | 1 |
| 1.: GENERAL REGISTRANT INFORMATION | 1 |
| 3.: INFORMATION ON MANUFACTURE AND USE(S) OF THE SUBSTANCE(S) | 2 |
| 6.: INFORMATION ON EXPOSURE FOR SUBSTANCES REGISTERED IN QUANTITIES BETWEEN 1 AND 10 TONNES PER YEAR PER MANUFATCURER OR IMPORTER | 5 |
| ANNEX VII: STANDARD INFORMATION REQUIREMENTS FOR SUBSTANCES MANUFACTURED OR IMPORTED IN QUANTITIES OF ONE TONNE OR MORE | |
| 8.: TOXICOLOGICAL INFORMATION | 1 |
| ANNEX VIII: STANDARD INFORMATION REQUIREMENTS FOR SUBSTANCES MANUFACTURED OR IMPORTED IN QUANTITIES OF 10 TONNES OR MORE | |
| 8.: TOXICOLOGICAL INFORMATION | 3 |
| 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 |
| 1.4.: In vitro methods | 1 |
| ANNEX XII: GENERAL PROVISIONS FOR DOWNSTREAM USERS TO ASSESS SUBSTANCES AND PREPARE CHEMICAL SAFETY REPORTS | |
| introduction: INTRODUCTION | 5 |
| ANNEX XIII: CRITERIA FOR THE IDENTIFICATION OF PERSISTENT, BIOACCUMULATIVE AND TOXIC SUBSTANCES, AND VERY PERSISTENT AND VERY BIOACCUMULATIVE SUBSTANCES | |
| 2.: SCREENING AND ASSESSMENT OF P, vP, B, vB and T PROPERTIES | |
| 2.1.: Registration | 1 |
| ANNEX XIV: LIST OF SUBSTANCES SUBJECT TO AUTHORISATION | 4 |
| ANNEX XV: DOSSIERS | |
| I.: INTRODUCTION AND GENERAL PROVISIONS | 1 |
| 2.: Dossier for the identification of a substance as a CMR, PBT, vPvB or a substance of equivalent concern according to Article 59 | 1 |
| 3.: Dossiers for restrictions proposal | 2 |
| ANNEX XVII: RESTRICTIONS ON THE MANUFACTURE, PLACING ON THE MARKET AND USE OF CERTAIN DANGEROUS SUBSTANCES, MIXTURES AND ARTICLES | 79 |
| Appendices 1 to 6 | |
| explanations of column headings: Explanations of column headings | 1 |
| Appendix 7: Special provisions on the labelling of articles containing asbestos | 4 |
| Appendix 10: Entry 43 — Azocolourants — List of testing methods | 2 |