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../file-system/small/txt ../file-system/small/txt Legislation - REACH Regulation
<p>REACH Legislation</p>
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11/03/24
REACH- ja CLP-asetusten 
mukaista aineiden 
yksilöimistä ja nimeämistä 
koskevat toimintaohjeet REACH- ja CLP-asetusten mukaista aineiden yksilöimistä ja nimeämistä koskevat toimintaohjeet substance_id_fi.pdf (1.5 MBk)
REACH- ja CLP-asetusten mukaista aineiden yksilöimistä ja nimeämistä koskevat toimintaohjeet
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22/02/24
Ainete REACH- ja CLPmääruse kohase 
identifitseerimise ja 
nimetamise juhend Ainete REACH- ja CLPmääruse kohase identifitseerimise ja nimetamise juhend substance_id_et.pdf (1.5 MBk)
Ainete REACH- ja CLPmääruse kohase identifitseerimise ja nimetamise juhend
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22/02/24
Documento de orientación 
para la identificación y 
denominación de las 
sustancias en REACH y CLP Documento de orientación para la identificación y denominación de las sustancias en REACH y CLP substance_id_es.pdf (1.5 MBk)
Documento de orientación para la identificación y denominación de las sustancias en REACH y CLP
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22/02/24
Καθοδήγηση σχετικά με τον
προσδιορισμό και την
ονοματοδοσία ουσιών
δυνάμει των κανονισμών
REACH και CLP Καθοδήγηση σχετικά με τον προσδιορισμό και την ονοματοδοσία ουσιών δυνάμει των κανονισμών REACH και CLP substance_id_el.pdf (1.7 MBk)
Καθοδήγηση σχετικά με τον προσδιορισμό και την ονοματοδοσία ουσιών δυνάμει των κανονισμών REACH και CLP
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22/02/24
Leitlinien zur Identifizierung 
und Bezeichnung von Stoffen 
gemäß REACH und CLP Leitlinien zur Identifizierung und Bezeichnung von Stoffen gemäß REACH und CLP substance_id_de.pdf (1.6 MBk)
Leitlinien zur Identifizierung und Bezeichnung von Stoffen gemäß REACH und CLP
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22/02/24
Vejledning om identifikation 
og navngivning af stoffer i 
henhold til REACH og CLP Vejledning om identifikation og navngivning af stoffer i henhold til REACH og CLP substance_id_da.pdf (1.5 MBk)
Vejledning om identifikation og navngivning af stoffer i henhold til REACH og CLP
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22/02/24
Pokyny pro identifikaci a  pojmenovávání látek podle nařízení REACH a CLP Pokyny pro identifikaci a pojmenovávání látek podle nařízení REACH a CLP substance_id_cs.pdf (1.6 MBk)
Pokyny pro identifikaci a pojmenovávání látek podle nařízení REACH a CLP
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22/02/24
Ръководство за идентифициране и именуване на веществата по REACH и CLP Ръководство за идентифициране и именуване на веществата по REACH и CLP substance_id_bg.pdf (1.8 MBk)
Ръководство за идентифициране и именуване на веществата по REACH и CLP
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22/02/24
Vägledning om identifiering och namngivning av ämnen enligt Reach och CLP Vägledning om identifiering och namngivning av ämnen enligt Reach och CLP substance_id_sv.pdf (1.5 MBk)
Vägledning om identifiering och namngivning av ämnen enligt Reach och CLP
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22/02/24
Smernice za identifikacijo in poimenovanje snovi v skladu z uredbama REACH in CLP Smernice za identifikacijo in poimenovanje snovi v skladu z uredbama REACH in CLP substance_id_sl.pdf (1.5 MBk)
Smernice za identifikacijo in poimenovanje snovi v skladu z uredbama REACH in CLP
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22/02/24
Usmernenie k identifikácii a pomenovaniu látok podľa nariadení REACH a CLP Usmernenie k identifikácii a pomenovaniu látok podľa nariadení REACH a CLP substance_id_sk.pdf (1.6 MBk)
Usmernenie k identifikácii a pomenovaniu látok podľa nariadení REACH a CLP
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22/02/24
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22/02/24
Guia de orientação para a 
identificação e designação de 
substâncias no âmbito dos 
Regulamentos REACH e CRE Guia de orientação para a identificação e designação de substâncias no âmbito dos Regulamentos REACH e CRE substance_id_pt.pdf (1.5 MBk)
Guia de orientação para a identificação e designação de substâncias no âmbito dos Regulamentos REACH e CRE
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22/02/24
Poradnik dotyczący 
identyfikacji i nazywania 
substancji na podstawie 
rozporządzeń REACH i CLP Poradnik dotyczący identyfikacji i nazywania substancji na podstawie rozporządzeń REACH i CLP substance_id_pl.pdf (1.6 MBk)
Poradnik dotyczący identyfikacji i nazywania substancji na podstawie rozporządzeń REACH i CLP
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22/02/24
Richtsnoer voor identificatie 
en naamgeving van stoffen 
volgens REACH en CLP Richtsnoer voor identificatie en naamgeving van stoffen volgens REACH en CLP substance_id_nl.pdf (1.5 MBk)
Richtsnoer voor identificatie en naamgeving van stoffen volgens REACH en CLP
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22/02/24
Gwida għall-identifikazzjoni u lgħoti ta’ ismijiet lil sustanzi taħt 
REACH u CLP Gwida għall-identifikazzjoni u lgħoti ta’ ismijiet lil sustanzi taħt REACH u CLP substance_id_mt.pdf (1.7 MBk)
Gwida għall-identifikazzjoni u lgħoti ta’ ismijiet lil sustanzi taħt REACH u CLP
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22/02/24
Vadlīnijas par vielu 
identificēšanu un nosaukumu 
piešķiršanu saskaņā ar 
REACH un CLP Vadlīnijas par vielu identificēšanu un nosaukumu piešķiršanu saskaņā ar REACH un CLP substance_id_lv.pdf (1.6 MBk)
Vadlīnijas par vielu identificēšanu un nosaukumu piešķiršanu saskaņā ar REACH un CLP
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22/02/24
Rekomendacijos dėl cheminių
medžiagų identifikavimo ir 
pavadinimo joms suteikimo 
pagal REACH ir CLP 
reglamentų reikalavimus Rekomendacijos dėl cheminių medžiagų identifikavimo ir pavadinimo joms suteikimo pagal REACH ir CLP reglamentų reikalavimus substance_id_lt.pdf (1.6 MBk)
Rekomendacijos dėl cheminių medžiagų identifikavimo ir pavadinimo joms suteikimo pagal REACH ir CLP reglamentų reikalavimus
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22/02/24
Guida per l’identificazione e la 
denominazione delle sostanze 
in ambito REACH e CLP Guida per l’identificazione e la denominazione delle sostanze in ambito REACH e CLP substance_id_it.pdf (1.5 MBk)
Guida per l’identificazione e la denominazione delle sostanze in ambito REACH e CLP
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22/02/24
Útmutató az anyagoknak a 
REACH- és a CLP-rendelet 
szerinti azonosításához és 
megnevezéséhez Útmutató az anyagoknak a REACH- és a CLP-rendelet szerinti azonosításához és megnevezéséhez substance_id_hu.pdf (1.6 MBk)
Útmutató az anyagoknak a REACH- és a CLP-rendelet szerinti azonosításához és megnevezéséhez
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22/02/24
Smjernice za identifikaciju i nazive tvari prema Uredbama REACH i CLP
Verzija 1.3. Smjernice za identifikaciju i nazive tvari prema Uredbama REACH i CLP Verzija 1.3. substance_id_hr.pdf (1.5 MBk)
Smjernice za identifikaciju i nazive tvari prema Uredbama REACH i CLP Verzija 1.3.
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22/02/24
../file-system/small/txt ../file-system/small/txt Creating your registration dossier
After you have compiled all the information on your substance necessary for fulfilling the REACH requirements, you need to document your findings in a registration dossier. The file that you submit...
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15/02/24
Important Note on EC Numbers and List Numbers: Some substances returned via the search above did not previously have an EC Number assigned, or were contained in a dossier for which a registrant did...
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15/02/24
Útmutató az intermedierekhez Útmutató az intermedierekhez intermediates_hu.pdf (1.6 MBk)
Útmutató az intermedierekhez
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01/02/24
Smjernice o intermedijerima Smjernice o intermedijerima intermediates_hr.pdf (1.5 MBk)
Smjernice o intermedijerima
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01/02/24
Richtsnoer over tussenproducten Richtsnoer over tussenproducten intermediates_nl.pdf (1.5 MBk)
Richtsnoer over tussenproducten
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01/02/24
Guia de orientação sobre substâncias intermédias Guia de orientação sobre substâncias intermédias intermediates_pt.pdf (1.5 MBk)
Guia de orientação sobre substâncias intermédias
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01/02/24
Vägledning rörande intermediärer Vägledning rörande intermediärer intermediates_sv.pdf (1.5 MBk)
Vägledning rörande intermediärer
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01/02/24
Leitlinien zu Zwischenprodukten Leitlinien zu Zwischenprodukten intermediates_de.pdf (1.5 MBk)
Leitlinien zu Zwischenprodukten
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01/02/24
Smernice za intermediate Smernice za intermediate intermediates_sl.pdf (1.5 MBk)
Smernice za intermediate
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01/02/24
Vejledning om mellemprodukter Vejledning om mellemprodukter intermediates_da.pdf (1.4 MBk)
Vejledning om mellemprodukter
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01/02/24
Pokyny pro meziprodukty Pokyny pro meziprodukty intermediates_cs.pdf (1.5 MBk)
Pokyny pro meziprodukty
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01/02/24
Καθοδήγηση σχετικά με τα ενδιάμεσα προϊόντα Καθοδήγηση σχετικά με τα ενδιάμεσα προϊόντα intermediates_el.pdf (1.6 MBk)
Καθοδήγηση σχετικά με τα ενδιάμεσα προϊόντα
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01/02/24
Orientaciones sobre sustancias intermedias Orientaciones sobre sustancias intermedias intermediates_es.pdf (1.4 MBk)
Orientaciones sobre sustancias intermedias
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01/02/24
Välituotteita koskevat toimintaohjeet Välituotteita koskevat toimintaohjeet intermediates_fi.pdf (1.4 MBk)
Välituotteita koskevat toimintaohjeet
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01/02/24
Guide sur les intermédiaires Guide sur les intermédiaires intermediates_fr.pdf (1.5 MBk)
Guide sur les intermédiaires
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01/02/24
Guida alle sostanze intermedie Guida alle sostanze intermedie intermediates_it.pdf (1.5 MBk)
Guida alle sostanze intermedie
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01/02/24
Rekomendacijos dėl tarpinių cheminių medžiagų Rekomendacijos dėl tarpinių cheminių medžiagų intermediates_lt.pdf (1.6 MBk)
Rekomendacijos dėl tarpinių cheminių medžiagų
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01/02/24
Vadlīnijas par starpproduktiem Vadlīnijas par starpproduktiem intermediates_lv.pdf (1.5 MBk)
Vadlīnijas par starpproduktiem
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01/02/24
Gwida dwar sustanzi intermedji Gwida dwar sustanzi intermedji intermediates_mt.pdf (1.6 MBk)
Gwida dwar sustanzi intermedji
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01/02/24
Ghid pentru intermediari Ghid pentru intermediari intermediates_ro.pdf (1.5 MBk)
Ghid pentru intermediari
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01/02/24
Usmernenia k medziproduktom Usmernenia k medziproduktom intermediates_sk.pdf (1.5 MBk)
Usmernenia k medziproduktom
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01/02/24
Ръководство за междинните продукти Ръководство за междинните продукти intermediates_bg.pdf (1.6 MBk)
Ръководство за междинните продукти
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01/02/24
Vaheainete juhend Vaheainete juhend intermediates_et.pdf (1.4 MBk)
Vaheainete juhend
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01/02/24
Poradnik na temat półproduktów Poradnik na temat półproduktów intermediates_pl.pdf (1.5 MBk)
Poradnik na temat półproduktów
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01/02/24
Dissemination and Confidentiality under REACH Regulation Dissemination and Confidentiality under REACH Regulation manual_dissemination_en.pdf (1.1 MBk)
Dissemination and Confidentiality under REACH Regulation
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29/01/24
Guidance on intermediates Guidance on intermediates intermediates_en.pdf (1.5 MBk)
Guidance on intermediates
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26/01/24
Guidance on the Application of the CLP Criteria Guidance on the Application of the CLP Criteria clp_en.pdf (12.9 MBk)
Guidance on the Application of the CLP Criteria
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16/01/24
Guidance for identification and naming of substances under REACH and CLP Guidance for identification and naming of substances under REACH and CLP substance_id_en.pdf (1.5 MBk)
Guidance for identification and naming of substances under REACH and CLP
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18/12/23
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
Rekisteröintiä koskevat toimintaohjeet Rekisteröintiä koskevat toimintaohjeet registration_fi.pdf (1.1 MBk)
Rekisteröintiä koskevat toimintaohjeet
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01/02/22
Registreerimisjuhend Registreerimisjuhend registration_et.pdf (1 MBk)
Registreerimisjuhend
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01/02/22
Orientaciones sobre el registro Orientaciones sobre el registro registration_es.pdf (1.2 MBk)
Orientaciones sobre el registro
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01/02/22
Καθοδήγηση σχετικά με την καταχώριση Καθοδήγηση σχετικά με την καταχώριση registration_el.pdf (1.4 MBk)
Καθοδήγηση σχετικά με την καταχώριση
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01/02/22
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 CLP
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14/12/21
Support Creating your registration dossier How to prepare registration and PPORD dossiers Guidance on registration Submitting your registration dossier What information you need
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14/12/21
Support Guidance on registration
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14/12/21
See also under the Legislation section Evaluation Registration
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14/12/21
Support Dossier evaluation decisions Guidance on registration Substance evaluation decisions
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13/12/21
Support Dissemination and Confidentiality under the REACH Regulation How to prepare an inquiry dossier What information you need
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13/12/21
Support Guidance on registration
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13/12/21
See also under the Legislation section Inquiry
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13/12/21
See also under the Legislation section Evaluation
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13/12/21
Guidance on Registration Guidance on Registration registration_en.pdf (1.4 MBk)
Guidance on Registration
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17/08/21
../file-system/small/txt ../file-system/small/txt Understanding REACH
REACH is a regulation of the European Union, adopted to improve the protection of human health and the environment from the risks that can be posed by chemicals, while enhancing the competitiveness...
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02/08/21
../file-system/small/txt ../file-system/small/txt Content pages - Subscribe
Follow us Read ECHA Weekly news Subscribe to our news
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08/04/21
Manufacturers, importers and downstream users based in the EU can submit a request for the use of an alternative chemical name to ECHA. It is not possible to appoint a ‘Third Party Representative’...
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08/03/21
../file-system/small/txt ../file-system/small/txt PPORD
If your substance is subject to product and process orientated research and development (PPORD), you can submit a PPORD notification to ECHA in order to be exempted from the obligation to register.
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04/03/21
../file-system/small/txt ../file-system/small/txt Registration - support
See also under the Support section Registration Questions and Answers on Registration
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25/02/21
Related Understanding CLP C&L Inventory How to submit and update your C&L notification Implementing Regulation (EU) 2020/1435
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22/02/21
Related Public activities coordination tool Substances of potential concern Examination of testing proposals Strategy for gathering your data Adaptations Good Laboratory Practice Dossier evaluation...
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22/02/21
../file-system/small/txt ../file-system/small/txt Recommendations - cnl box
Classification and labelling
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22/02/21
../file-system/small/txt ../file-system/small/txt Recommendations - adaptions box
Adaptations
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22/02/21
../file-system/small/txt ../file-system/small/txt Recommendations - registration
If your company manufactures or imports substances in quantities of more than one tonne per year, you are responsible for compiling and submitting a registration dossier to ECHA. The following...
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22/02/21
../file-system/small/txt ../file-system/small/txt What information you need to submit
As a registrant of a substance, you need to compile all the required information in a registration dossier, which has two main components: A technical dossier is always required for all substances...
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10/06/20
If you have prepared your registration dossier in IUCLID, you need to submit it to ECHA through REACH-IT. REACH-IT is the central IT system for companies to securely submit, process and manage...
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10/06/20
There are four steps in the process of data gathering before registering a substance. Agree with your co-registrants how to divide the work or whether to outsource some, or all of it. 1. Collect...
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10/06/20
Typically, tests are contracted out as a package. This has the advantage of being performed by experts in the most time-efficient manner and according to the required quality standards and legal...
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10/06/20
../file-system/small/txt ../file-system/small/txt In vitro methods main
A test performed in vitro ("in the glass") means that it is done outside of a living organism and it usually involves isolated tissues, organs or cells. You can use in vitro data to fully or partly...
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10/06/20
If you manufacture or import a substance in amounts less than one tonne a year, you do not need to register the substance. If you reach or exceed this threshold, your tonnage band will determine...
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10/06/20
../file-system/small/txt ../file-system/small/txt inforeq 10 to 100 main
To register a substance in the 10 to 100 tonnage band, you need to provide information specified in Column 1 of REACH Annexes VII and VIII, comprising certain physicochemical data, toxicological...
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10/06/20
../file-system/small/txt ../file-system/small/txt inforeq 1 to 10 tonnes main
To register a substance in the 1 to 10 tonnage band, you need to provide information specified in Column 1 of REACH Annex VII, including certain physicochemical data, toxicological information and...
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10/06/20
If you only have a few substances to manage, you can take advantage of the IUCLID Cloud to create your dossiers in the IUCLID format. To use the service, you will need an ECHA account and to...
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10/06/20
Under REACH, testing on vertebrate animals (e.g. rats, other mammals or fish) can only be used as a last resort to fulfil information requirements for registration. There are multiple ways to avoid...
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10/06/20
../file-system/small/txt ../file-system/small/txt From submission to decision
ECHA assigns a submission number to each received dossier. This number is used as a reference in all correspondence relating to this registration until a registration number is assigned. Dossier...
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10/06/20
../file-system/small/txt ../file-system/small/txt Finding your co-registrants
You will need to share data and register your substance jointly with other companies. In practice, this means that you need to: Submit an inquiry via REACH-IT to ask ECHA if you have...
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10/06/20
Claiming an “adaptation” means that it is possible to omit a test based on certain general rules or specific rules that apply for just one information requirement. General rules for adaptations can...
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10/06/20
../file-system/small/txt ../file-system/small/txt Collecting information on uses main
In your registration dossier you also have to report / provide information on how your substance is used in your supply chain. To retrieve such information you can use many sources, for example:...
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10/06/20
Demonstrating the safe use of your substance in a registration dossier requires a significant investment of time, money and expertise. You will need to have dialogue and, normally, contractual...
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10/06/20
Once you know the identity of your substance, you need to see if your substance needs to be registered or if it is exempt from registration. On ECHA’s website you can check if your substance is...
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10/06/20
../file-system/small/txt ../file-system/small/txt Do I need to register?
You need to determine whether it is you who needs to register a substance or another actor in your supply chain.
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10/06/20
Questions and Answers Pre-registration Inquiry Registration Joint submission NONS
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20/04/20
../file-system/small/txt ../file-system/small/txt dos and dont's table
These Dos and Don'ts can help make negotiations successful. Dos Don'ts Before the negotiations ✓ Establish and maintain clear contact details, if possible a functional electronic mailbox to...
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12/03/20
../file-system/small/txt ../file-system/small/txt What is IUCLID
IUCLID is a software to record, store, maintain and exchange data on intrinsic and hazard properties of chemical substances. ECHA co-develops the software with the OECD. Under REACH, information...
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12/03/20
../file-system/small/txt ../file-system/small/txt SMEs and consultants:See also
See also under the Legislation section Registration
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11/03/20
See also under the Legislation section Registration
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06/03/20
The following elements must be part of the data-sharing agreement: Data itemisation The existing registrant must provide information on the specific data to be shared. This information must allow...
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06/03/20
REACH requires existing registrants and potential registrants to make every effort to reach an agreement on sharing data. The legislation also requires that the costs of sharing the information for...
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06/03/20
Support Sector-specific support for substance identification Guidance on substance identification How to characterise and identify your substance Getting started with EU chemicals legislation...
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26/02/20
See also under the Legislation section Substance identification
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26/02/20
Related IT tools ECHA Cloud Services IUCLID 6 REACH-IT
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26/02/20
Support Registered substances database Lead registrant list Getting started with EU chemicals legislation Guidance on registration
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26/02/20
../file-system/small/txt ../file-system/small/txt RAAF links
Related Guidance on information requirements and chemical safety assessment, R.6 QSAR and grouping of chemicals The Read-across assessment framework [PDF] [EN] Human health: Appendix HH-A:...
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18/02/20
../file-system/small/txt ../file-system/small/txt Related documents
Related documents DCG recommendation on continued cooperation [PDF] Practical guide: How to report changes in identity of legal entities
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18/02/20
../file-system/small/txt ../file-system/small/txt Registration - obligations -links
Support Practical examples – REACH registration How to cooperate for REACH registration – best practice for SMEs and consultants
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18/02/20
5 Prepare your registration as a IUCLID dossier How to protect your confidential business information [PDF] These video tutorials highlight different aspects in preparing your technical dossier...
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18/02/20
4 Assess hazards and risks of substances These examples are based on real situations, and illustrate some recommended steps to gather the information you need to register a substance. They will...
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18/02/20
3 Get organised with your co-registrants Under REACH, the costs of data must be shared in a fair, transparent and non-discriminatory way. These documents will guide you on this. Sharing the costs...
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18/02/20
See also under Legislation section Data sharing Inquiry Registration Substance identification
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11/02/20
Related IT tools REACH-IT IUCLID
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11/02/20
See also under the Legislation section Registration Substance identification Inquiry Nanomaterials
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11/02/20
../file-system/small/txt ../file-system/small/txt From submission to decision related
See also under the Legislation section Publishing information from dossiers Safety Data Sheets Related documents How to prepare registration and PPORD dossiers Information on manual verification...
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11/02/20
See also under the Legislation section Registration Related documents Fact sheet: REACH-IT – what you need to know [PDF] [EN] Related IT tools REACH-IT Support What is REACH-IT SME fees under...
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11/02/20
Related Guidance on registration Guidance on information requirements and chemical safety assessment Guidance in a nutshell on chemical safety assessment [PDF] [EN] (Q)SARs and grouping of...
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11/02/20
See also under the Legislation section Information requirements Examination of testing proposals Chemical safety report Substance identification
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11/02/20
Support Questions and Answers on Information requirements, test methods and quality of data Testing methods and alternatives ECHA Information toolkit Exposure scenario examples Questions and...
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11/02/20
See also under the Legislation section Registration Addressing chemicals of concern
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11/02/20
../file-system/small/txt ../file-system/small/txt Related docs under in vitro methods
Related Practical guide on How to use alternatives to animal testing to fulfil your information requirements [PDF] [EN] Guidance on information requirements and chemical safety assessment, R.7...
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11/02/20
../file-system/small/txt ../file-system/small/txt Support under in vitro methods
Support European Union Reference Laboratory for alternatives to animal testing
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11/02/20
Related Practical guide on How to use alternatives to animal testing to fulfil your information requirements [PDF] [EN] Practical guide on How to use and report QSARs [PDF] [EN] Guidance on...
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11/02/20
../file-system/small/txt ../file-system/small/txt to avoid animal tests support links
Support Recommendations to registrants
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11/02/20
See also under the Legislation section Data-sharing Information requirements REACH legislation
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11/02/20
Support Monitoring impact of REACH on innovation, competitiveness and SMEs [PDF] [EN] What you need to consider for your business
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11/02/20
Related Practical guide for SME managers and REACH coordinators - - How to fulfil your information requirements at tonnages 1-10 and 10-100 tonnes per year [PDF] [EN]
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11/02/20
See also under the Legislation section Information requirements
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11/02/20
../file-system/small/txt ../file-system/small/txt Your registration obligations
There are three factors that determine whether or not you need to register your substance. You should look at each of these three factors for every substance you deal with: Your role in the supply...
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11/02/20
See also under the Legislation section Registration Information requirements Related IT tools ECHA Cloud Services IUCLID 6 REACH-IT
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11/02/20
See also under the Legislation section Inquiry Registration Substance identification
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11/02/20
See also under the Legislation section Registration
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11/02/20
../file-system/small/txt ../file-system/small/txt strategy for gathering data support
Support What information you need How to avoid unnecessary testing on animals Testing methods and alternatives Guidance on information requirements and chemical safety assessment National websites...
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10/02/20
Related Practical guide on How to use alternatives to animal testing to fulfil your information requirements [PDF] [EN] Practical guide on How to use and report QSAR [PDF] [EN] Practical...
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10/02/20
See also under the Legislation section REACH and related implementing legislation
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10/02/20
Related Practical guide on How to use alternatives to animal testing to fulfil your information requirements [PDF] [EN] Adaptation of information requirements (R.5) Practical guide for SME...
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10/02/20
Support Recommendations to registrants
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10/02/20
See also under the Legislation section Information requirements REACH legislation
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10/02/20
Related Practical guide for SME managers and REACH coordinators - How to fulfil your information requirements at tonnages 1-10 and 10-100 tonnes per year [PDF] [EN]
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10/02/20
../file-system/small/txt ../file-system/small/txt Related IT Tools
Related IT tools Chesar Video: Overview of Chesar
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10/02/20
../file-system/small/txt ../file-system/small/txt inforeq 100 more under regulations
See also under the Legislation section 10-100 tonnes requirements REACH legislation Dossier evaluation
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10/02/20
Related Practical guide for SME managers and REACH coordinators - How to fulfil your information requirements at tonnages 1-10 and 10-100 tonnes per year [PDF] [EN]
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10/02/20
Support Reduced information requirements (Annex III) Recommendations to registrants Guidance on Information Requirements and Chemical Safety Assessment
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10/02/20
../file-system/small/txt ../file-system/small/txt inforeq 10 more under regulations
See also under the Legislation section 1-10 tonnes requirements REACH legislation Dossier evaluation
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10/02/20
../file-system/small/txt ../file-system/small/txt what info you need support links
Support Guidance on information requirements and chemical safety assessment Recommendations to registrants Questions and Answers SMEs
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10/02/20
../file-system/small/txt ../file-system/small/txt what info you need related docs
Related Practical guide for SME managers and REACH coordinators - How to fulfil your information requirements at tonnages 1-10 and 10-100 tonnes per year [PDF] [EN]
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10/02/20
See also under the Legislation section Information requirements Substance Identification Dossier Evaluation Classification Chemical safety report
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10/02/20
../file-system/small/txt ../file-system/small/txt Need help - registered substances
See a problem or have feedback?
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30/01/20
../file-system/small/txt ../file-system/small/txt The registration process - see also
See also Manuals on preparing REACH and CLP dossiers List of MSCAs
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15/11/19
../file-system/small/txt ../file-system/small/txt Preparing and submitting an inquiry
Preparing and submitting an inquiry Before registering, you have a duty to prepare and submit an inquiry to ECHA. The inquiry process will take place before manufacturing or placing on the market....
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24/10/19
Standard information requirements
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23/05/19
../file-system/small/txt ../file-system/small/txt Recommendations - registration box
Registration
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23/05/19
../file-system/small/txt ../file-system/small/txt Recommendations - substance id box
Substance identification
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23/05/19