Hindamine
ECHA and the Member States evaluate the information submitted by companies to examine the quality of the registration dossiers and the testing proposals and to clarify if a given substance constitutes a risk to human health or the environment.
Evaluation under REACH focuses on three different areas:
- Examination of testing proposals submitted by registrants
- Compliance check of the dossiers submitted by registrants
- Substance evaluation
Once the evaluation is done, registrants may be required to submit further information on the substance.
REACH-määruse artikli 54 kohaselt on ECHA kohustatud avaldama iga aasta 28. veebruariks eelmisel aastal hindamiskohustustega seotud tegevuse aruande. ECHA-l on konkreetne kohustus lisada aruannetesse soovitused potentsiaalsetele registreerijatele, et parandada tulevaste registreerimiste kvaliteeti.
- Guidance on dossier and substance evaluation[PDF] [EN]
- Guidance on priority setting for evaluation[PDF] [EN]
- Guidance on registration[PDF] [EN]
- Guidance for identification and naming of substances[PDF] [EN]
- Guidance on data sharing[PDF] [EN]
- Guidance on the application of the CLP Criteria[PDF] [EN]
- Practical guide 1. How to report in vitro data[PDF] [EN]
- Practical guide 2. How to report weight of evidence[PDF] [EN]
- Practical guide 3. How to report robust study summaries[PDF] [EN]
- Practical guide 4. How to report data waiving[PDF] [EN]
- Practical guide 5. How to report (Q)SARs[PDF] [EN]
- Practical guide 6. How to report read-across and categories[PDF] [EN]
- Practical guide 10. How to avoid unnecessary testing on animals[PDF] [EN]
- Practical guide 12: How to communicate with ECHA in dossier evaluation[PDF] [EN]
- Practical Guide 14: How to prepare toxicological summaries in IUCLID and how to derive DNELs [PDF] [EN]
- Practical Guide 15: How to undertake a qualitative human health assessment and document it in a chemical safety report [PDF] [EN]
See also
- Title VI of the REACH Regulation (EC) No 1907/2006
- European Centre for the Validation of Alternative Methods (ECVAM)
- Webinars
- Member State Committee
- Information Toolkit
- ECHA's Procedure on Dossier Evaluation [PDF] [EN]
- Guidance on information requirements and chemical safety assessment
- Substance Evaluation fact sheet[PDF] [EN]