Registration
How to prepare an inquiry dossier
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03/11/23
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Registration
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03/11/23
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News2018
<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
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News2018
<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
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News2018
<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
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News2018
<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
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general
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
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Jobs
Information on manual verification at completeness check
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22/05/23
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general
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
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general
Support Registered substances C&L Inventory
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08/05/23
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general
Si prega di notare che l’allegato III è stato aggiornato dal regolamento (UE) 2018/1881, che modifica le disposizioni in considerazione dei nanomateriali [regolamento (UE) 2018/1881 della...
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08/05/23
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general
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
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general
Link correlati REACH-IT
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30/03/23
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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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27/03/23
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general
In una registrazione il dichiarante attesta la manipolazione sicura della sostanza in questione lungo tutta la catena di approvvigionamento, in modo da garantire la tutela della salute dell’uomo e...
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27/03/23
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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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16/03/23
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general
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
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general
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
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general
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
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general
Ai fini della registrazione, il dichiarante deve prima capire quali informazioni raccogliere per dimostrare l’uso sicuro della sostanza. Successivamente, deve riportare tali informazioni nel...
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14/02/23
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general
La classificazione e l’etichettatura rappresentano il punto di partenza per la comunicazione di informazioni sui pericoli e sono aspetti importanti per garantire che la salute umana e l’ambiente...
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09/02/23
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general
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
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general
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
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general
Tools for data submission REACH-IT IUCLID CHESAR
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06/10/22
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general
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
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general
Regulations REACH/PPORD
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04/10/22
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Registration
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
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Read-Across Assessment
Framework (RAAF)
raaf_en.pdf
(760 KBk)
Registration
Read-Across Assessment
Framework (RAAF)
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05/08/22
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general
I dati provengono dai fascicoli di registrazione presentati all'ECHA entro la data indicata come ultimo aggiornamento. La fascia totale di tonnellaggio è compilata a partire da tutti i fascicoli,...
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18/05/22
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Registration
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
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general
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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general
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
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Registration
Guidance on Registration
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01/02/22
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Registration
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01/02/22
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Registration
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01/02/22
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Registration
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01/02/22
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Registration
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01/02/22
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Registration
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01/02/22
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Registration
Usmernenia k registrácii
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01/02/22
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Registration
Ghid privind înregistrarea
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01/02/22
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Registration
Guia de orientação sobre o registo
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01/02/22
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Registration
Poradnik na temat rejestracji
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01/02/22
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01/02/22
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Registration
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01/02/22
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Registration
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01/02/22
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01/02/22
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SMJERNICE
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Svibanj 2012.
Verzija 2.0
Smjernice za provedbu Uredbe REACH
registration_hr.pdf
(1,3 MBk)
Registration
SMJERNICE
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Svibanj 2012.
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Registration
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01/02/22
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