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TITLE I: GENERAL ISSUES
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CHAPTER 2: Definitions and general provision
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Article 3: Definitions
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2 |
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TITLE II: REGISTRATION OF SUBSTANCES
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CHAPTER 1: General obligation to register and information requirements
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Article 10: Information to be submitted for general registration purposes
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4 |
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Article 11: Joint submission of data by multiple registrants
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7 |
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Article 12: Information to be submitted depending on tonnage
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1 |
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Article 13: General requirements for generation of information on intrinsic properties of substances
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3 |
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Article 14: Chemical safety report and duty to apply and recommend risk reduction measures
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5 |
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CHAPTER 3: Obligation to register and information requirements for certain types of isolated intermediates
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Article 17: Registration of on-site isolated intermediates
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1 |
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Article 18: Registration of transported isolated intermediates
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1 |
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Article 19: Joint submission of data on isolated intermediates by multiple registrants
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1 |
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CHAPTER 4: Common provisions for all registrations
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Article 20: Duties of the Agency
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7 |
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Article 21: Manufacturing and import of substances
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5 |
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Article 22: Further duties of registrants
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5 |
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TITLE III: DATA SHARING AND AVOIDANCE OF UNNECESSARY TESTING
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CHAPTER 2: Rules for non-phase-in substances and registrants of phase-in substances who have not pre-registered
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Article 26: Duty to inquire prior to registration
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7 |
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Article 27: Sharing of existing data in the case of registered substances
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23 |
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CHAPTER 3: Rules for phase-in-substances
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Article 28: Duty to pre-register for phase-in substances
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2 |
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Article 30: Sharing of data involving tests
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3 |
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TITLE IV: INFORMATION IN THE SUPPLY CHAIN
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Article 36: Obligation to keep information
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3 |
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TITLE VI: EVALUATION
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CHAPTER 1: Dossier evaluation
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Article 40: Examination of testing proposals
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3 |
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Article 41: Compliance check of registrations
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2 |
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CHAPTER 2: Substance evaluation
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Article 46: Requests for further information and check of information submitted
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2 |
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Article 48: Follow-up to substance evaluation
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1 |
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CHAPTER 3: Evaluation of intermediates
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Article 49: Further information on on-site isolated intermediates
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1 |
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CHAPTER 4: Common provisions
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Article 50: Registrants' and downstream users' rights
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10 |
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Article 51: Adoption of decisions under dossier evaluation
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1 |
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Article 52: Adoption of decisions under substance evaluation
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1 |
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Article 53: Cost sharing for tests without an agreement between registrants and/or downstream users
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2 |
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TITLE XII: INFORMATION
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Article 119: Electronic public access
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1 |
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ANNEX I: GENERAL PROVISIONS FOR ASSESSING SUBSTANCES AND PREPARING CHEMICAL SAFETY REPORTS
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1.: HUMAN HEALTH HAZARD ASSESSMENT
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1.3.: Step 3: Classification and Labelling
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1 |
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2.: PHYSICOCHEMICAL HAZARD ASSESSMENT
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1 |
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3.: ENVIRONMENTAL HAZARD ASSESSMENT
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3.2.: Step 2: Classification and Labelling
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1 |
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ANNEX II: REQUIREMENTS FOR THE COMPILATION OF SAFETY DATA SHEETS
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1.: SECTION 1: Identification of the substance/mixture and of the company/undertaking
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1.1.: Product identifier
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1 |
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3.: SECTION 3: Composition/information on ingredients
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3.2.: Mixtures
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1 |
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ANNEX VI: INFORMATION REQUIREMENTS REFERRED TO IN ARTICLE 10
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STEP 1: GATHER AND SHARE EXISTING INFORMATION
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3 |
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STEP 2: CONSIDER INFORMATION NEEDS
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1 |
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STEP 3: IDENTIFY INFORMATION GAPS
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1 |
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notes: NOTES
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1 |
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1.: GENERAL REGISTRANT INFORMATION
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2 |
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3.: INFORMATION ON MANUFACTURE AND USE(S) OF THE SUBSTANCE(S)
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2 |
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ANNEX VII: STANDARD INFORMATION REQUIREMENTS FOR SUBSTANCES MANUFACTURED OR IMPORTED IN QUANTITIES OF ONE TONNE OR MORE
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2 |
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9.: ECOTOXICOLOGICAL INFORMATION
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1 |
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ANNEX VIII: STANDARD INFORMATION REQUIREMENTS FOR SUBSTANCES MANUFACTURED OR IMPORTED IN QUANTITIES OF 10 TONNES OR MORE
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2 |
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8.: TOXICOLOGICAL INFORMATION
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3 |
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9.: ECOTOXICOLOGICAL INFORMATION
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1 |
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ANNEX IX: STANDARD INFORMATION REQUIREMENTS FOR SUBSTANCES MANUFACTURED OR IMPORTED IN QUANTITIES OF 100 TONNES OR MORE
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4 |
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8.: TOXICOLOGICAL INFORMATION
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5 |
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9.: ECOTOXICOLOGICAL INFORMATION
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3 |
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ANNEX X: STANDARD INFORMATION REQUIREMENTS FOR SUBSTANCES MANUFACTURED OR IMPORTED IN QUANTITIES OF 1 000 TONNES OR MORE
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4 |
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8.: TOXICOLOGICAL INFORMATION
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6 |
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9.: ECOTOXICOLOGICAL INFORMATION
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3 |
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ANNEX XI: GENERAL RULES FOR ADAPTATION OF THE STANDARD TESTING REGIME SET OUT IN ANNEXES VII TO X
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1 |
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ANNEX XIII: CRITERIA FOR THE IDENTIFICATION OF PERSISTENT, BIOACCUMULATIVE AND TOXIC SUBSTANCES, AND VERY PERSISTENT AND VERY BIOACCUMULATIVE SUBSTANCES
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2.: SCREENING AND ASSESSMENT OF P, vP, B, vB and T PROPERTIES
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2.1.: Registration
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