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Registration dossiers for the 2018 Deadline Registration dossiers for the 2018 Deadline Registration dossiers for the 2018 Deadline (375.4k)
# Registrations % # Substances Registrations in Joint Submissions 15 494 96% 6 304 Lead 4 310 28% 4,189 Member 11 184 72% 3,232 Individual Registrations under REACH ...
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23/02/18
REACH 2018 - support links REACH 2018 - support links REACH 2018
Support Help for exceptional situations (DCG solutions) REACH 2018 events calendar Toolkit for promoting the REACH 2018 registration deadline Contact ECHA's accredited...
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22/02/18
Legislation - REACH Regulation Legislation - REACH Regulation Legislation
REACH Regulation Consolidated version of the REACH Regulation The consolidated version of the Regulation (EC) No 1907/2006 of the European Parliament and of the Council on the...
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20/02/18
Registration statistics - technical notes Registration statistics - technical notes Technical notes
Substance phase-in/non phase-in status and NONS allocation At the registration level phase-in/non phase-in status is derived by the status indicated by the company in the...
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20/02/18
Registration statistics - overview of all countries Registration statistics - overview of all countries Registration statistics - overview of all countries (91.1k)
Registration Statistics # Registrations # Substances Registrations in Joint Submissions 50 500 9 497 Lead 10 056 N/A Member 40 444 N/A Individual Registrations...
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20/02/18
Helping registrants in exceptional cases Helping registrants in exceptional cases Helping registrants in exceptional cases
true News release 9999 false ECHA/NR/18/06 Companies facing exceptional situations that are likely to prevent them from registering on time should inform ECHA ahead of the...
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20/02/18
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16/02/18
News Watch a webinar: Guided dossier preparation in IUCLID Cloud, 14 February 2018 IUCLID Cloud now guides you through dossier preparation, 19 December 2017 Watch webinar Best...
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16/02/18
Assess hazards and risks of substances - practical examples Assess hazards and risks of substances - practical examples Practical examples – REACH 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...
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08/02/18
300 people gather in Helsinki for last minute advice ahead of the final registration deadline for chemicals 300 people gather in Helsinki for last minute advice ahead of the final registration deadline for chemicals 300 people gather in Helsinki for last minute advice ahead of the final registration deadline for chemicals
true Press release 2 false ECHA/PR/18/02 The European Chemicals Agency will host over 300 participants from industry, academia and authorities from all over the world for its...
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02/02/18
Non-EU Countries - Kosovo Non-EU Countries - Kosovo Non-EU/EEA countries
Kosovo Ministry of Environment and Spatial Planning Leaflet (AL) Leaflet (SR) Leaflet (EN) This designation is without prejudice to positions on status and is in line with...
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18/12/17
Toolkit for promoting the registration deadline Toolkit for promoting the registration deadline Toolkit for promoting the registration deadline
Does your organisation interact with manufacturers and importers of chemicals who need to register by 31 May 2018? Or, with users of chemicals who need to make sure their uses...
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07/12/17
Support Chemical Watch's REACH consortia database Lead registrant list News List of substances with lead registrants available, 28 September 2016 REACH 2018: Find your...
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04/12/17
working together - support working together - support Disputes in practice
Support Letter template for data-sharing and joint submission negotiations [.docx] [EN] Questions and answers on data sharing Information to be shared for registration...
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28/11/17
Upcoming Follow the Directors' Contact Group developments Support Letter template for data-sharing and joint submission negotiations [.docx] News Guidance on data sharing,...
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28/11/17
to avoid animal testing related docs to avoid animal testing related docs How to avoid unnecessary testing on animals
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]...
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21/11/17
Webinar: IUCLID Cloud - Best practice for service providers and SMEs Webinar: IUCLID Cloud - Best practice for service providers and SMEs Webinar: IUCLID Cloud - Best practice for service providers and SMEs
20171129020000 Chemical Watch Online Free webinar 15:00 - 16:00 Helsinki time (EET, GMT +2) aimed at consultants working with SMEs. Webinar: IUCLID Cloud - Best practice for...
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20/11/17
Information on manual verification at completeness check Information on manual verification at completeness check Information on manual verification at completeness check (335.0k)
18 October 2017 1 Information on manual verification at completeness check ECHA performs a completeness check on each incoming registration to ensure that...
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25/10/17
Guidance in a nutshell - Scientific Research and Development (SR&D), Product and Process Orientated Research and Development (PPORD) Guidance in a nutshell - Scientific Research and Development (SR&D), Product and Process Orientated Research and Development (PPORD) Guidance in a nutshell - Scientific Research and Development (SR&D), Product and Process Orientated Research and Development (PPORD) (415.0k)
G U I D A N C E I N A N U T S H E L L Scientific Research and Development (SR&D), Product and Process Orientated Research and Development (PPORD) The document aims...
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19/10/17
Guidance on Scientific Research and Development (SR&D) and Product and Process Oriented Research and Development (PPORD) Guidance on Scientific Research and Development (SR&D) and Product and Process Oriented Research and Development (PPORD) Guidance on Scientific Research and Development (SR&D) and Product and Process Oriented Research and Development (PPORD) (620.6k)
G U I D A NC E Guidance on Scientific Research and Development (SR&D) and Product and Process Orientated Research and Development (PPORD) Version 2.1 October 2017...
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19/10/17
Assess hazard and risk webinar Assess hazard and risk webinar Assess hazard and risk
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18/10/17
reach2018 Denmark reach2018 Denmark member states
Denmark Miljø- og Fødevareministeriet, Miljøstyrelsen REACH Registering
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18/10/17
How to create your registration dossier with the IUCLID Cloud How to create your registration dossier with the IUCLID Cloud How to create your registration dossier with IUCLID cloud
If you are an SME or a consultant for an SME, you can take advantage of the IUCLID Cloud for SMEs to create your dossier in the IUCLID format. To use the service, you will need...
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09/10/17
Understanding REACH Understanding REACH 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...
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07/10/17
From submisison to decision link box From submisison to decision link box Registration
From submisison to decision
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04/10/17
Upcoming Evaluation under REACH, Progress Report 2017 News Study finds companies lack incentives for updating their REACH registrations, 4 September 2017 Important safety...
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03/10/17
Requesting an alternative chemical name in mixtures-Links Requesting an alternative chemical name in mixtures-Links Requesting a review of a decision on the use of an alternative chemical name
Related MB/17/2011: Decision Amending Decision MB/17/2008 establishing remedies for reviewing a partial or full rejection of a confidentiality request pursuant to Article 118(3)...
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19/09/17
How to create a registration dossier with IUCLID cloud link box How to create a registration dossier with IUCLID cloud link box Creating your registration dossier
How to create a registration dossier with the IUCLID Cloud for SMEs
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18/09/17
What information you need to submit What information you need to submit What 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...
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15/09/17
Related Joint submission of data
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04/09/17
REACH 2018 events navi REACH 2018 events navi events
February 2017 | March 2017 | April 2017 | May 2017 June 2017 | July 2017 | August 2017 | September 2017 | October 2017 | November 2017 | January 2018
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31/08/17
Reduced information requirements - how to check the benefits Reduced information requirements - how to check the benefits Reduced information requirements
How to check if you benefit from reduced information requirements The following steps will help you check whether your substance can be registered with information only on its...
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28/08/17
Form for describing the manufacturing process of UVCB substances 1 (2) August 2017 Annankatu 18, P.O. Box 400, FI-00121 Helsinki, Finland | Tel. +358...
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25/08/17
[Document title] 3 (4) Internal/Restricted/Confidential XX/xx dd Month yyyy Form for describing the manufacturing process of UVCB substances 1...
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25/08/17
Under REACH, there is no obligation to register substances in amounts below one tonne a year. To further encourage innovation, substances used in scientific research and...
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25/08/17
Adaptations to the standard information requirements related documents Adaptations to the standard information requirements related documents Adaptations to the standard information requirements
Related Practical guide on How to use alternatives to animal testing to fulfil your information requirements Adaptation of information requirements (R.5) Practical guide for...
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18/08/17
Information requirements 10 to 100 tonnes per year related documents Information requirements 10 to 100 tonnes per year related documents Information requirements: 10 to 100 tonnes per year
Related Guidance in a nutshell on chemical safety assessment Chesar in a nutshell [PDF] [EN] Practical guide for SME managers and REACH coordinators [PDF] [EN]
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18/08/17
Related docs under in vitro methods Related docs under in vitro methods In vitro methods
Related Guidance on information requirements and chemical safety assessment, R.7 Endpoint specific guidance
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17/08/17
Related documents under qsar models Related documents under qsar models QSAR models
Related Guidance on information requirements and chemical safety assessment, R.6 QSAR and grouping of chemicals
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17/08/17
strategy for gathering data related docs strategy for gathering data related docs Strategy for gathering your data
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]...
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17/08/17
what info you need related docs what info you need related docs What information you need
Related Guidance on information requirements and chemical safety assessment, R.2 Information requirements Practical guide for SME managers and REACH coordinators [PDF] [EN]
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17/08/17
How to change your substance identifier - related links How to change your substance identifier - related links How to change your substance identifier
Related Webform
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17/08/17
Information required for registration Information required for registration Information to be shared for registration
Related Information requirements: 1-10 tonnes a year Information requirements: 10-100 tonnes a year
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15/08/17
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:...
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15/08/17
How to improve your dossier - sidelinks How to improve your dossier - sidelinks Lessons learnt from dossier evaluation
Related Substance identity Compliance check Evaluation decisions Registration CSR/ES Roadmap Guidance
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11/08/17
Requesting an alternative chemical name in mixtures-Links Requesting an alternative chemical name in mixtures-Links Requesting an alternative chemical name in mixtures
Related Directive 2000/39/EC of 8 June 2000 establishing a first list of indicative occupational exposure limit values [PDF] [EN] Directive 2006/15/EC of 7 February 2006...
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10/08/17
PPORD - related documents PPORD - related documents PPORD
Related Manual: How to prepare registration and submit a PPORD dossier notification Template for reporting justification for the request for extension [DOC] [EN]
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10/08/17
REACH 2018 - Upcoming REACH 2018 - Upcoming Know your portfolio
Support Contact your national REACH helpdesk or the ECHA helpdesk Form on the manufacturing process of UVCB substances [PDF] [Word file] News Last push to raise awareness about...
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10/08/17
Registration - related documents Registration - related documents Registration
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...
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01/08/17
Guidance in a nutshell Registration data and dossier handling Guidance in a nutshell Registration data and dossier handling Guidance in a nutshell Registration data and dossier handling (731.5k)
G U I D A N C E I N A N U T S H E L L Registration The document aims to explain in simple terms the registration obligations and briefly summarises the parent...
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05/07/17

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