Read-Across Assessment
Framework (RAAF)
raaf_en.pdf
(760 KBk)
Registration
Read-Across Assessment
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05/08/22
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general
REACH Legislation
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29/06/22
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In this table, you will find all public data submitted to ECHA in REACH registration dossiers by substance manufacturers, importers, or their representatives, as laid out by the REACH Regulation...
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18/05/22
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Jobs
Information on manual verification at completeness check
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16/05/22
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Support Practical guide on how to use alternatives to animal testing [PDF] [EN] Practical guide on how to use and report (Q)SARs [PDF] [EN] QSAR Toolbox examples Manual on How to...
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05/05/22
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Related Adaptations How to avoid animal testing Practical guide on how to use and report QSARs Grouping of substances and read-across Advice on using read-across for UVCB substances [EN] [PDF]
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04/05/22
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Registration
Please note: We have successfully adapted to the latest IUCLID format, and have resumed processing dossiers since 3 March 2022. Over the coming weeks we will catch up with the backlog of...
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04/04/22
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general
Implementing Legislation Regulation on the duties placed on registrants to update their registrations under Regulation (EC) No 1907/2006 of the European Parliament and of the Council concerning the...
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23/03/22
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RELATED INFORMATION Registered substances information How to determine what will be published (Data Submission Manual 15) Understanding REACH Regulation Q&A on registered substances What is an...
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24/02/22
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Related CLP Legislation Commission Regulation amending REACH annexes VII to XI Implementing legislation on dossier updates IT screening campaigns on dossiers REACH Legislation Upcoming changes to...
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Related Practical Guide on How to act in dossier evaluation Evaluation process Dossier evaluation status Fact sheet: Follow up to dossier evaluation decisions [PDF]
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Guidance on Registration
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Pokyny pro registraci
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Ghid privind înregistrarea
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SMJERNICE
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Verzija 2.0
Smjernice za provedbu Uredbe REACH
registration_hr.pdf
(1.3 MBk)
Registration
SMJERNICE
Smjernice za registraciju
Svibanj 2012.
Verzija 2.0
Smjernice za provedbu Uredbe REACH
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Rekisteröintiä koskevat toimintaohjeet
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Καθοδήγηση σχετικά με την καταχώριση
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Dossier evaluation
Related Information requirements Practical guide for SME managers and REACH coordinators - How to fulfil your information requirements at tonnages 1-10 and 10-100 tonnes per year Guidance on...
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Support Dissemination and confidentiality under the REACH Regulation Guidance on registration How do I claim a registration number for a NONS How to act in dossier or substance evaluation How to...
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Support ECHA Accounts manual for Industry Users Guidance on registration How to act in dossier or substance evaluation How to cease manufacture How to report changes in identity under REACH and...
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Support Dossier evaluation decisions Guidance on registration Substance evaluation decisions
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Support Dissemination and Confidentiality under the REACH Regulation How to prepare an inquiry dossier What information you need
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See also under the Legislation section Inquiry
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See also under the Legislation section Evaluation
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The registration dossier has to reflect the current knowledge on how your substance can be used safely at production sites and by users throughout the supply chain. This means that after you have...
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26/11/21
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Support Chemical Watch's REACH consortia database How to prepare and develop a Substance Identity Profile (SIP) [PDF] [EN] News List of substances with lead registrants available, 28...
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19/08/21
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Data sharing
Guidance on Registration
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