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How to prepare an inquiry dossier How to prepare an inquiry dossier manual_inquiry_en.pdf (1.8 MBk)
How to prepare an inquiry dossier
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03/11/23
How to prepare registration and PPORD dossiers How to prepare registration and PPORD dossiers manual_regis_and_ppord_en.pdf (4.4 MBk)
How to prepare registration and PPORD dossiers
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03/11/23
<p>Registration numbers have been granted to 32 515 dossiers out of the 33 363 dossiers that were submitted by the final REACH registration deadline on 31 May. These registrations cover 10 708...
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16/10/23
<p>Submit your REACH 2018 registration dossier before the end of March and receive ECHA’s decision on your registration within three weeks. If you make your submission in April or May, it may take...
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16/10/23
<p>Companies facing exceptional situations that are likely to prevent them from registering on time should inform ECHA ahead of the deadline of 31 May 2018.</p>
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16/10/23
<p>The European Chemicals Agency will host over 300 participants from industry, academia and authorities from all over the world for its REACH 2018 Stakeholders’ Day on 31 January. The event marks...
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16/10/23
Support ECHA's Questions and answers 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...
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01/06/23
Information on manual verification at completeness check Information on manual verification at completeness check manual_completeness_check_en.pdf (339 KBk)
Information on manual verification at completeness check
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22/05/23
Related IUCLID Manual: How to prepare registration and PPORD dossiers Guidance on Information Requirements and Chemical Safety Assessment, Chapter R2, Chapter R12
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08/05/23
Support Registered substances C&L Inventory
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08/05/23
../file-system/small/txt ../file-system/small/txt Annex III modification
Annex III has been modified by Regulation 2018/1881, modifying provisions in case of nanomaterials (Commission Regulation (EU) 2018/1881 of 3 December 2018 amending Regulation (EC) No 1907/2006 of...
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08/05/23
../file-system/small/txt ../file-system/small/txt Reduced information requirements
If you manufacture or import your phase-in substance between 1-10 tonnes per year, you may be able to register it with a reduced set of information, covering only its physicochemical properties....
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08/05/23
../file-system/small/txt ../file-system/small/txt Registration - related documents
Related ECHA's REACH 2018 Roadmap [PDF] [EN] Guidance on registration [PDF] [EN] Guidance in a nutshell on registration [PDF] [EN] Guidance on requirements for substances in articles
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30/03/23
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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27/03/23
../file-system/small/txt ../file-system/small/txt Support - Registration
In a registration you show that the substance you deal with is handled safely throughout the supply chain, ensuring that human health and the environment are protected. You provide this information...
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27/03/23
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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16/03/23
Related Practical Guide on How to act in dossier evaluation Evaluation process Dossier evaluation status Fact sheet: Follow up to dossier evaluation decisions [PDF] Questions and Answers about...
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28/02/23
Related Substance evaluation – CoRAP table Substance evaluation Evaluation process Practical guide on how to act in substance evaluation Community rolling action plan Questions and answers
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28/02/23
../file-system/small/txt ../file-system/small/txt Recommendations - adaptions related
Related Adaptations to the standard information requirements How to avoid unnecessary testing on animals Practical guide: "How to use and report (Q)SARs" Guidance on information requirements and...
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28/02/23
../file-system/small/txt ../file-system/small/txt what info you need top text
<p>To be ready for registration, you first need to understand what information you have to collect to demonstrate the safe use of your substance. You then report this information in your...
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14/02/23
../file-system/small/txt ../file-system/small/txt Recommendations - cnl
Classification and labelling is the starting point for hazard communication and an important element in making sure that human health and the environment are protected from harmful chemicals....
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09/02/23
Related Chesar website Guidance on chemical safety assessment (including parts B and D) Chemical safety report EScom standard (Cefic) Sector use map formats
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09/02/23
Related Substance identification process under REACH Substance identification – get started Guidance on substance identification How to prepare registrations for nanomaterials [PDF] Advice on using...
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01/02/23
../file-system/small/txt ../file-system/small/txt Data submission tools
Tools for data submission REACH-IT IUCLID CHESAR
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06/10/22
Related Commission Directive (EU) 2019/1831 of 24 October 2019 establishing a fifth list of indicative occupational exposure limit values Commission Directive (EU) 2017/164 of 31 January 2017...
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05/10/22
../file-system/small/txt ../file-system/small/txt PPORD - regulations
Regulations REACH/PPORD
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04/10/22
Please note: As of end June 2022 we have processed and published all dossiers that had been pending since 14 October 2021. While daily processing has resumed there remains a processing queue. New...
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16/08/22
Read-Across Assessment
Framework (RAAF) Read-Across Assessment Framework (RAAF) raaf_en.pdf (760 KBk)
Read-Across Assessment Framework (RAAF)
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05/08/22
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
../file-system/small/txt ../file-system/small/txt avoid animal tests subpages support
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 prepare...
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05/05/22
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
../file-system/small/txt ../file-system/small/txt Registration - related documents
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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11/02/22
Guidance on Registration Guidance on Registration registration_de.pdf (1.2 MBk)
Guidance on Registration
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01/02/22
Vejledning om registrering Vejledning om registrering registration_da.pdf (1.1 MBk)
Vejledning om registrering
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01/02/22
Pokyny pro registraci Pokyny pro registraci registration_cs.pdf (1.4 MBk)
Pokyny pro registraci
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01/02/22
Ръководство за регистрация Ръководство за регистрация registration_bg.pdf (1.4 MBk)
Ръководство за регистрация
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01/02/22
Vägledning om registrering Vägledning om registrering registration_sv.pdf (1 MBk)
Vägledning om registrering
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01/02/22
Smernice za registracijo Smernice za registracijo registration_sl.pdf (1.3 MBk)
Smernice za registracijo
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01/02/22
Usmernenia k registrácii Usmernenia k registrácii registration_sk.pdf (1.4 MBk)
Usmernenia k registrácii
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01/02/22
Ghid privind înregistrarea Ghid privind înregistrarea registration_ro.pdf (1.4 MBk)
Ghid privind înregistrarea
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01/02/22
Guia de orientação sobre o registo Guia de orientação sobre o registo registration_pt.pdf (1.2 MBk)
Guia de orientação sobre o registo
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01/02/22
Poradnik na temat rejestracji Poradnik na temat rejestracji registration_pl.pdf (1.4 MBk)
Poradnik na temat rejestracji
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01/02/22
Richtsnoer over registratie Richtsnoer over registratie registration_nl.pdf (1.2 MBk)
Richtsnoer over registratie
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01/02/22
Guidance on Registration Guidance on Registration registration_mt.pdf (1.5 MBk)
Guidance on Registration
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01/02/22
Reģistrācijas vadlīnijas Reģistrācijas vadlīnijas registration_lv.pdf (1.3 MBk)
Reģistrācijas vadlīnijas
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01/02/22
Rekomendacijos dėl registracijos Rekomendacijos dėl registracijos registration_lt.pdf (1.3 MBk)
Rekomendacijos dėl registracijos
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01/02/22
Guida alla registrazione Guida alla registrazione registration_it.pdf (1.1 MBk)
Guida alla registrazione
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01/02/22
Útmutató a regisztráláshoz Útmutató a regisztráláshoz registration_hu.pdf (1.4 MBk)
Útmutató a regisztráláshoz
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01/02/22
SMJERNICE
Smjernice za registraciju
Svibanj 2012.
Verzija 2.0
Smjernice za provedbu Uredbe REACH SMJERNICE Smjernice za registraciju Svibanj 2012. Verzija 2.0 Smjernice za provedbu Uredbe REACH registration_hr.pdf (1.3 MBk)
SMJERNICE Smjernice za registraciju Svibanj 2012. Verzija 2.0 Smjernice za provedbu Uredbe REACH
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01/02/22
Guide de l'enregistrement Guide de l'enregistrement registration_fr.pdf (1.2 MBk)
Guide de l'enregistrement
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01/02/22