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Read-Across Assessment Framework (RAAF) - scenario 3 Read-Across Assessment Framework (RAAF) - scenario 3 Read-Across Assessment Framework (RAAF) - scenario 3 (173.7k)
Read-Across Assessment Framework (RAAF) 1 Appendix C: Scenario 3 1.1 DESCRIPTION This scenario covers the category approach for which the read-across hypothesis is based on...
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22/05/15
Read-Across Assessment Framework (RAAF) - scenario 2 Read-Across Assessment Framework (RAAF) - scenario 2 Read-Across Assessment Framework (RAAF) - scenario 2 (202.4k)
Read-Across Assessment Framework (RAAF) 1 Appendix B: Scenario 2 1.1 DESCRIPTION This scenario covers the analogue approach for which the read-across hypothesis is based on...
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22/05/15
Read-Across Assessment Framework (RAAF) - scenario 1 Read-Across Assessment Framework (RAAF) - scenario 1 Read-Across Assessment Framework (RAAF) - scenario 1 (177.3k)
Read-Across Assessment Framework (RAAF) 1 Appendix A: Scenario 1 1.1 DESCRIPTION This scenario covers the analogue approach for which the read-across hypothesis is based on...
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22/05/15
Read-Across Assessment Framework (RAAF) - scenario 6 Read-Across Assessment Framework (RAAF) - scenario 6 Read-Across Assessment Framework (RAAF) - scenario 6 (202.9k)
Read-Across Assessment Framework (RAAF) 1 Appendix F: Scenario 6 1.1 DESCRIPTION This scenario covers the category approach for which the read-across hypothesis is based on...
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22/05/15
Registration Statistics REACH 2013 Registration Statistics REACH 2013 Registration Statistics REACH 2013 (169.1k)
REACH 2013 - Overview Status on 10 September 2013 The REACH deadline for registering substances manufactured or imported in quantities of 100 to 1 000 tonnes per year was...
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20/04/15
ECHA’s REACH 2018 Roadmap ECHA’s REACH 2018 Roadmap ECHA’s REACH 2018 Roadmap (434.7k)
ECHA’s REACH 2018 Roadmap 14 January 2015 ECHA’s REACH 2018 Roadmap2 ECHA’s REACH 2018 Roadmap Reference: ECHA-15-R-01-EN Catalogue number: ED-07-14-106-EN-N ISBN: ...
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14/01/15
Registered substances - registered substances Registered substances - registered substances Registered substances information
As substances are registered under REACH, there is an obligation on registrants to provide information on the substances they manufacture or import. ECHA subsequently has the...
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01/10/14
IT screening campaigns on dossiers - substance id related news IT screening campaigns on dossiers - substance id related news IT screening campaigns on dossiers
Related news e-News 09 April 2014ECHA targets substance identity – letters sent to companies with shortcomings in their registrations News Alert 11 December 2013 Is your...
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17/09/14
How to improve your dossier - webinars table How to improve your dossier - webinars table Related webinars
Webinar related to dossier quality Content Date Substance identity issues covered in the screening campaign Concentration ranges Compositions with no constituents No...
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31/07/14
Practical Guide 16: How to assess whether a substance is used as an intermediate under strictly controlled conditions and how to report the information for the intermediate registration in IUCLID Practical Guide 16: How to assess whether a substance is used as an intermediate under strictly controlled conditions and how to report the information for the intermediate registration in IUCLID Practical Guide 16: How to assess whether a substance is used as an intermediate under strictly controlled conditions and how to report the information for the intermediate registration in IUCLID (1,932.3k)
How to assess whether a substance is used as an intermediate under strictly controlled conditions and how to report the information for the intermediate registration in...
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25/06/14
Directors’ Contact Group first edition (4 June 2014) Checklist to hire a good consultant Directors’ Contact Group first edition (4 June 2014) Checklist to hire a good consultant Directors’ Contact Group first edition (4 June 2014) Checklist to hire a good consultant (137.2k)
1 DIRECTORS’ CONTACT GROUP FIRST EDITION (4 June 2014) CHECKLIST TO HIRE A GOOD CONSULTANT I. Internal preparation work II. Personal criteria of a...
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10/06/14
Directors’ Contact Group final (4 June 2014) Considerations to be made when joining an existing SIEF Directors’ Contact Group final (4 June 2014) Considerations to be made when joining an existing SIEF Directors’ Contact Group final (4 June 2014) Considerations to be made when joining an existing SIEF (185.1k)
1 DIRECTORS’ CONTACT GROUP FINAL (4 June 2014) CONSIDERATIONS TO BE MADE WHEN JOINING AN EXISTING SIEF Below are some considerations to be borne in...
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10/06/14
How to improve your dossier - lessons from dossier evaluation intro How to improve your dossier - lessons from dossier evaluation intro Lessons learnt from dossier evaluation
In line with Article 54 of REACH, by 28 February of each year, ECHA publishes a report on the progress it has made over the previous calendar year in relation to evaluation. In...
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02/05/14
ANNEX to the information letter about Substance Identity issues found in your registration dossier ANNEX to the information letter about Substance Identity issues found in your registration dossier ANNEX to the information letter about Substance Identity issues found in your registration dossier (2,724.4k)
Annex to SID information letter 1 (21) 07 April 2014 Annankatu 18, P.O. Box 400, FI-00121 Helsinki, Finland | Tel. +358 9 686180 | Fax +358 9 68618210 |...
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08/04/14
Dossier Quality Assistant overview of rules Dossier Quality Assistant overview of rules Dossier Quality Assistant overview of rules (296.6k)
1 • This document gives an overview of the rules covered by the Dossier Quality Assistant (DQA), which is incorporated in the IUCLID Validation Assistant plug-in. The rules...
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06/03/14
The registration dossier - Q&As The registration dossier - Q&As The registration dossier
Questions and Answers Questions and Answers on Joint Submission of data by multiple registrants Questions and Answers on Information requirements, test methods and quality of data
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24/02/14
Template for reporting justification for the request for extension - To be attached to section 1.9 of the IUCLID 5 dossier Template for reporting justification for the request for extension - To be attached to section 1.9 of the IUCLID 5 dossier Template for reporting justification for the request for extension - To be attached to section 1.9 of the IUCLID 5 dossier (76.5k)
Annex A: Research & Development information provided in order to justify the request for extension of a PPORD notification To be attached to section 1.9 of the IUCLID 5...
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26/07/13
Read-across illustrative example Part 2 Example 1 – Analogue approach: similarity based on breakdown products Read-across illustrative example Part 2 Example 1 – Analogue approach: similarity based on breakdown products Read-across illustrative example Part 2 Example 1 – Analogue approach: similarity based on breakdown products (468.8k)
Annankatu 18, P.O. Box 400, FI-00121 Helsinki, Finland | Tel. +358 9 686180 | Fax +358 9 68618210 | echa.europa.eu Read-across illustrative example Part 2 Example 1 –...
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15/04/13
Grouping of substances and read-across approach Part 1: Introductory note Grouping of substances and read-across approach Part 1: Introductory note Grouping of substances and read-across approach Part 1: Introductory note (396.4k)
Annankatu 18, P.O. Box 400, FI-00121 Helsinki, Finland | Tel. +358 9 686180 | Fax +358 9 68618210 | echa.europa.eu Grouping of substances and read-across approach Part 1:...
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15/04/13
Screening of registration dossiers for intermediates - Background information Screening of registration dossiers for intermediates - Background information Screening of registration dossiers for intermediates - Background information (84.4k)
1 (2) 13 September 2012 Annankatu 18, P.O. Box 400, FI-00121 Helsinki, Finland | Tel. +358 9 686180 | Fax +358 9 68618210 | echa.europa.eu Screening of...
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14/09/12
Leaflet - Request for use of an Alternative Chemical Name Leaflet - Request for use of an Alternative Chemical Name Leaflet - Request for use of an Alternative Chemical Name (288.1k)
ECHA-11-L-07-EN Request for use of an Alternative Chemical Name Manufacturers, importers and downstream users who wish to produce or import a mixture – e.g....
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12/09/12
Decision establishing remedies for reviewing a partial or full rejection of a confidentiality request Decision establishing remedies for reviewing a partial or full rejection of a confidentiality request Decision establishing remedies for reviewing a partial or full rejection of a confidentiality request (27.0k)
Helsinki, 23 April 2008 Doc: MB/17/2008 final1 DECISION ESTABLISHING REMEDIES FOR REVIEWING A PARTIAL OR FULL REJECTION OF A CONFIDENTIALITY ...
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12/04/12
Decision amending decision mb/17/2008 establishing remedies for reviewing a partial or full rejection of a confidentiality request pursuant to article 118(3) of regulation (ec) no 1907/2006 Decision amending decision mb/17/2008 establishing remedies for reviewing a partial or full rejection of a confidentiality request pursuant to article 118(3) of regulation (ec) no 1907/2006 Decision amending decision mb/17/2008 establishing remedies for reviewing a partial or full rejection of a confidentiality request pursuant to article 118(3) of regulation (ec) no 1907/2006 (45.9k)
1 Helsinki, 22 June 2011 Doc: MB/17/2011 final DECISION AMENDING DECISION MB/17/2008 ESTABLISHING REMEDIES FOR...
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05/12/11
Guidance on intermediates Guidance on intermediates Guidance on intermediates (1,274.1k)
Guidance on intermediates Version: 2 December 2010 LEGAL NOTICE This document contains guidance on REACH explaining the REACH...
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29/11/11
Registration statistics 2010 Registration statistics 2010 Registration statistics 2010 (36.3k)
This report covers the number of dossiers submitted between 1 January and 30 November 2010 The final number of registrations and substances will be available when all...
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29/11/11

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