Évaluation
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.
Conformément à l'article 54 du règlement REACH, l'ECHA doit publier chaque année, avant le 28 février, un rapport sur les progrès réalisés au cours de l'année civile écoulée dans l'exécution des obligations qui lui incombent en ce qui concerne l'évaluation. L'ECHA est plus particulièrement tenue d'inclure dans ces rapports des recommandations aux déclarants potentiels afin d'améliorer la qualité des futurs enregistrements.
- 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]