general
<p>REACH Legislation</p>
Similar Results
|
11/03/24
|
REACH- ja CLP-asetusten
mukaista aineiden
yksilöimistä ja nimeämistä
koskevat toimintaohjeet
substance_id_fi.pdf
(1.5 MBk)
Registration
REACH- ja CLP-asetusten
mukaista aineiden
yksilöimistä ja nimeämistä
koskevat toimintaohjeet
Similar Results
|
22/02/24
|
Ainete REACH- ja CLPmääruse kohase
identifitseerimise ja
nimetamise juhend
substance_id_et.pdf
(1.5 MBk)
Information requirements
Ainete REACH- ja CLPmääruse kohase
identifitseerimise ja
nimetamise juhend
Similar Results
|
22/02/24
|
Documento de orientación
para la identificación y
denominación de las
sustancias en REACH y CLP
substance_id_es.pdf
(1.5 MBk)
Information requirements
Documento de orientación
para la identificación y
denominación de las
sustancias en REACH y CLP
Similar Results
|
22/02/24
|
Καθοδήγηση σχετικά με τον
προσδιορισμό και την
ονοματοδοσία ουσιών
δυνάμει των κανονισμών
REACH και CLP
substance_id_el.pdf
(1.7 MBk)
Information requirements
Καθοδήγηση σχετικά με τον
προσδιορισμό και την
ονοματοδοσία ουσιών
δυνάμει των κανονισμών
REACH και CLP
Similar Results
|
22/02/24
|
Leitlinien zur Identifizierung
und Bezeichnung von Stoffen
gemäß REACH und CLP
substance_id_de.pdf
(1.6 MBk)
Information requirements
Leitlinien zur Identifizierung
und Bezeichnung von Stoffen
gemäß REACH und CLP
Similar Results
|
22/02/24
|
Vejledning om identifikation
og navngivning af stoffer i
henhold til REACH og CLP
substance_id_da.pdf
(1.5 MBk)
Information requirements
Vejledning om identifikation
og navngivning af stoffer i
henhold til REACH og CLP
Similar Results
|
22/02/24
|
Pokyny pro identifikaci a pojmenovávání látek podle nařízení REACH a CLP
substance_id_cs.pdf
(1.6 MBk)
Information requirements
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
substance_id_bg.pdf
(1.8 MBk)
Information requirements
Ръководство за идентифициране и именуване на веществата по REACH и CLP
Similar Results
|
22/02/24
|
Vägledning om identifiering och namngivning av ämnen enligt Reach och CLP
substance_id_sv.pdf
(1.5 MBk)
Information requirements
Vägledning om identifiering och namngivning av ämnen enligt Reach och CLP
Similar Results
|
22/02/24
|
Smernice za identifikacijo in poimenovanje snovi v skladu z uredbama REACH in CLP
substance_id_sl.pdf
(1.5 MBk)
Information requirements
Smernice za identifikacijo in poimenovanje snovi v skladu z uredbama REACH in CLP
Similar Results
|
22/02/24
|
Usmernenie k identifikácii a pomenovaniu látok podľa nariadení REACH a CLP
substance_id_sk.pdf
(1.6 MBk)
Information requirements
Usmernenie k identifikácii a pomenovaniu látok podľa nariadení REACH a CLP
Similar Results
|
22/02/24
|
Information requirements
Similar Results
|
22/02/24
|
Guia de orientação para a
identificação e designação de
substâncias no âmbito dos
Regulamentos REACH e CRE
substance_id_pt.pdf
(1.5 MBk)
Information requirements
Guia de orientação para a
identificação e designação de
substâncias no âmbito dos
Regulamentos REACH e CRE
Similar Results
|
22/02/24
|
Poradnik dotyczący
identyfikacji i nazywania
substancji na podstawie
rozporządzeń REACH i CLP
substance_id_pl.pdf
(1.6 MBk)
Information requirements
Poradnik dotyczący
identyfikacji i nazywania
substancji na podstawie
rozporządzeń REACH i CLP
Similar Results
|
22/02/24
|
Richtsnoer voor identificatie
en naamgeving van stoffen
volgens REACH en CLP
substance_id_nl.pdf
(1.5 MBk)
Information requirements
Richtsnoer voor identificatie
en naamgeving van stoffen
volgens REACH en CLP
Similar Results
|
22/02/24
|
Gwida għall-identifikazzjoni u lgħoti ta’ ismijiet lil sustanzi taħt
REACH u CLP
substance_id_mt.pdf
(1.7 MBk)
Information requirements
Gwida għall-identifikazzjoni u lgħoti ta’ ismijiet lil sustanzi taħt
REACH u CLP
Similar Results
|
22/02/24
|
Vadlīnijas par vielu
identificēšanu un nosaukumu
piešķiršanu saskaņā ar
REACH un CLP
substance_id_lv.pdf
(1.6 MBk)
Information requirements
Vadlīnijas par vielu
identificēšanu un nosaukumu
piešķiršanu saskaņā ar
REACH un CLP
Similar Results
|
22/02/24
|
Rekomendacijos dėl cheminių
medžiagų identifikavimo ir
pavadinimo joms suteikimo
pagal REACH ir CLP
reglamentų reikalavimus
substance_id_lt.pdf
(1.6 MBk)
Information requirements
Rekomendacijos dėl cheminių
medžiagų identifikavimo ir
pavadinimo joms suteikimo
pagal REACH ir CLP
reglamentų reikalavimus
Similar Results
|
22/02/24
|
Guida per l’identificazione e la
denominazione delle sostanze
in ambito REACH e CLP
substance_id_it.pdf
(1.5 MBk)
Information requirements
Guida per l’identificazione e la
denominazione delle sostanze
in ambito REACH e CLP
Similar Results
|
22/02/24
|
Útmutató az anyagoknak a
REACH- és a CLP-rendelet
szerinti azonosításához és
megnevezéséhez
substance_id_hu.pdf
(1.6 MBk)
Information requirements
Útmutató az anyagoknak a
REACH- és a CLP-rendelet
szerinti azonosításához és
megnevezéséhez
Similar Results
|
22/02/24
|
Smjernice za identifikaciju i nazive tvari prema Uredbama REACH i CLP
Verzija 1.3.
substance_id_hr.pdf
(1.5 MBk)
Information requirements
Smjernice za identifikaciju i nazive tvari prema Uredbama REACH i CLP
Verzija 1.3.
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|
22/02/24
|
general
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
|
general
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
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Registration
Útmutató az intermedierekhez
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01/02/24
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Registration
Smjernice o intermedijerima
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01/02/24
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Registration
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01/02/24
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Guia de orientação sobre substâncias intermédias
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01/02/24
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01/02/24
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Registration
Leitlinien zu Zwischenprodukten
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01/02/24
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Registration
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01/02/24
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Registration
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01/02/24
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01/02/24
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Registration
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01/02/24
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Registration
Orientaciones sobre sustancias intermedias
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01/02/24
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Registration
Välituotteita koskevat toimintaohjeet
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01/02/24
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Registration
Guide sur les intermédiaires
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01/02/24
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Registration
Guida alle sostanze intermedie
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01/02/24
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Registration
Rekomendacijos dėl tarpinių cheminių medžiagų
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01/02/24
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Registration
Vadlīnijas par starpproduktiem
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01/02/24
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Registration
Gwida dwar sustanzi intermedji
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01/02/24
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Registration
Ghid pentru intermediari
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01/02/24
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Registration
Usmernenia k medziproduktom
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01/02/24
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Registration
Ръководство за междинните продукти
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01/02/24
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Registration
Vaheainete juhend
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|
01/02/24
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Registration
Poradnik na temat półproduktów
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01/02/24
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Registration
Dissemination and Confidentiality under REACH Regulation
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29/01/24
|
Registration
Guidance on intermediates
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26/01/24
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Guidance on the Application of the CLP Criteria
clp_en.pdf
(12.9 MBk)
Classification Labelling Packaging
Guidance on the Application of the CLP Criteria
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16/01/24
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Guidance for identification and naming of substances under REACH and CLP
substance_id_en.pdf
(1.5 MBk)
Information requirements
Guidance for identification and naming of substances under REACH and CLP
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18/12/23
|
Registration
How to prepare an inquiry dossier
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03/11/23
|
Registration
How to prepare registration and PPORD dossiers
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03/11/23
|
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
|
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
|
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
|
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
|
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
|
Jobs
Information on manual verification at completeness check
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22/05/23
|
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
|
general
Support Registered substances C&L Inventory
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08/05/23
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general
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
|
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
|
general
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
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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
|
general
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
|
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
|
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
|
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
|
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
|
general
<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
|
general
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
|
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
|
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
|
general
Tools for data submission REACH-IT IUCLID CHESAR
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06/10/22
|
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
|
general
Regulations REACH/PPORD
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04/10/22
|
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
|
Read-Across Assessment
Framework (RAAF)
raaf_en.pdf
(760 KBk)
Registration
Read-Across Assessment
Framework (RAAF)
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05/08/22
|
general
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
|
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
|
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
|
Registration
Guidance on Registration
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01/02/22
|
Registration
Vejledning om registrering
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01/02/22
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Registration
Pokyny pro registraci
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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
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01/02/22
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Registration
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01/02/22
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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
Guida alla registrazione
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01/02/22
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Registration
Útmutató a regisztráláshoz
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01/02/22
|
SMJERNICE
Smjernice za registraciju
Svibanj 2012.
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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01/02/22
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Registration
Guide de l'enregistrement
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01/02/22
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Registration
Rekisteröintiä koskevat toimintaohjeet
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01/02/22
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Registration
Registreerimisjuhend
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01/02/22
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Registration
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01/02/22
|
Registration
Καθοδήγηση σχετικά με την καταχώριση
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01/02/22
|
general
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
|
general
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
|
general
Support Guidance on registration
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14/12/21
|
general
See also under the Legislation section Evaluation Registration
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|
14/12/21
|
general
Support Dossier evaluation decisions Guidance on registration Substance evaluation decisions
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13/12/21
|
general
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
|
general
Support Guidance on registration
Similar Results
|
13/12/21
|
general
See also under the Legislation section Inquiry
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|
13/12/21
|
general
See also under the Legislation section Evaluation
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|
13/12/21
|
Data sharing
Guidance on Registration
Similar Results
|
17/08/21
|
general
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
|
Active substance approval
Follow us Read ECHA Weekly news Subscribe to our news
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|
08/04/21
|
Registration
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
PPORD
Registration
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.
Similar Results
|
04/03/21
|
Registration
See also under the Support section Registration Questions and Answers on Registration
Similar Results
|
25/02/21
|
Dossier evaluation
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
|
Dossier evaluation
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
|
Dossier evaluation
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|
22/02/21
|
Dossier evaluation
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|
22/02/21
|
Dossier evaluation
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
|
Registration
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...
Similar Results
|
10/06/20
|
Registration
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
|
Registration
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
|
Registration
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
|
Registration
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
|
Registration
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
|
Registration
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
|
Registration
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
|
Registration
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
|
Registration
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
|
Registration
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
|
Registration
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
|
Registration
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
|
Registration
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
|
Registration
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
|
Registration
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
|
Registration
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
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Registration
Questions and Answers Pre-registration Inquiry Registration Joint submission NONS
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20/04/20
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Registration
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
|
Registration
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
|
Registration
See also under the Legislation section Registration
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11/03/20
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Registration
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06/03/20
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Registration
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
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Registration
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
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26/02/20
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See also under the Legislation section Substance identification
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18/02/20
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Registration
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18/02/20
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18/02/20
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18/02/20
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Registration
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
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Registration
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
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Registration
See also under Legislation section Data sharing Inquiry Registration Substance identification
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11/02/20
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Registration
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11/02/20
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Registration
See also under the Legislation section Registration Substance identification Inquiry Nanomaterials
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11/02/20
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Registration
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11/02/20
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Registration
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11/02/20
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Registration
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11/02/20
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Registration
See also under the Legislation section Information requirements Examination of testing proposals Chemical safety report Substance identification
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11/02/20
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Registration
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11/02/20
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11/02/20
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11/02/20
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11/02/20
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Registration
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11/02/20
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11/02/20
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11/02/20
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Registration
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11/02/20
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Registration
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
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Registration
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10/02/20
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Registration
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10/02/20
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Registration
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Registration
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10/02/20
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See also under the Legislation section Information requirements Substance Identification Dossier Evaluation Classification Chemical safety report
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10/02/20
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30/01/20
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Registration
See also Manuals on preparing REACH and CLP dossiers List of MSCAs
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15/11/19
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Registration
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
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Dossier evaluation
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23/05/19
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Dossier evaluation
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