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Applications for Authorisation
SEAC/62/2024/01 - SEAC’S RECOMMENDATION ON REVIEW PERIOD
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27/03/24
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general
<p>REACH Legislation</p>
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11/03/24
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general
<p>To better plan the committees' workload, ECHA establishes specific windows for submitting applications for authorisation. Uploading your application within these windows can ensure the minimum...
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20/02/24
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general
Current submission windows Submission window - (corresponding latest application date) Substances 2013 20 May – 3 June Submission window available for all substances 7 - 21 August (21 August 2013)...
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20/02/24
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general
Applications for authorisation can cover uses of an authorised substance of very high concern (SVHC) by the applying company, by downstream users further down in the supply chain, or both....
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23/01/24
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general
<p><script type="application/javascript" defer src="https://europa.eu/webtools/load.js"></script>
<script type="application/json">{
"service": "charts",
"version": "2.0",
"data": {
...
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19/01/24
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general
31 December 2023 Downstream uses notified (active) Uses for which own authorisation is held*) Total authorised uses Bis(2-ethylhexyl)phthalate (DEHP) 8 2 10 bis(2-methoxyethyl) ether 2 11 13...
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16/01/24
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Applications for Authorisation
Reference DNELs RAC 33 diglyme
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06/11/23
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Applications for Authorisation
SEAC/24/2014/04
(Agreed at SEAC-24)
Evaluation of restriction reports and applications for
authorisation for PBT and vPvB substances in SEAC
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30/06/23
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general
Implementing Legislation Regulation on the duties placed on registrants to update their registrations under Regulation (EC) No 1907/2006 of the European Parliament and of the Council concerning the...
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16/03/23
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general
Future applicants for authorisation may request a teleconference based information session (TIS) with ECHA to clarify regulatory and procedural issues related to the authorisation application...
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02/03/23
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How the Committee for Socio-Economic Analysis will evaluate
economic feasibility in applications for authorisation
EIGHTEENTH MEETING OF THE COMMITTEE FOR SOCIO-ECONOMIC ANALYSIS
6-8 MARCH 2013
HELSINKI, FINLAND
Concerns: Authorisations - Economic feasibility
Agenda Point: 6a
Action requested: For agreement
seac_authorisations_economic_feasibility_evaluation_en.pdf
(80 KBk)
Applications for Authorisation
How the Committee for Socio-Economic Analysis will evaluate
economic feasibility in applications for authorisation
EIGHTEENTH MEETING OF THE COMMITTEE FOR SOCIO-ECONOMIC ANALYSIS
6-8 MARCH 2013...
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17/01/23
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Applications for Authorisation
Documents on how applications are treated and evaluated including the reference DNELs or dose-response relationships. While the documents relate to the Committees' evaluation of applications,...
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19/12/22
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general
Includes only substances for which there are upstream authorisations, i.e. authorisations applied for by the manufacturers and importers of chemicals covering their downstream uses and sometimes...
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17/08/22
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general
Related Socio-economic impacts of REACH authorisations (2017) [PDF] [EN] Authorisation process Addressing substances of concern Report of the AfA task force 2017 [PDF] [EN] Report of the AfA task...
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20/04/22
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Applications for Authorisation
Fee calculator XLS file
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19/04/22
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general
1 An application/review report is received in terms of Article 64(1) of REACH when ECHA has received the application fee. 2 One opinion refers to a compiled version of the final opinions of RAC and...
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29/03/22
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general
Disclaimer: These examples illustrate different practices of how applications for authorisation have been prepared. They are neither endorsed by, nor should they be considered as binding on, the...
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25/03/22
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general
Related links Comitology register European Commission: Authorisation decisions Downstream uses covered by granted authorisations Status of Authorisation decisions [XLSX] (updated 31/12/2021)
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02/02/22
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general
Further information ECHA Fee calculator [XLSX] ECHA Helpdesk Management Board decision MB/D/29/2010 – Decision on the classification of services for which charges are levied [PDF] [EN]
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31/01/22
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Applications for Authorisation
Comments submitted to date
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14/01/22
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general
Related Substitution to safer chemicals Authorisation supply chain coverage [PDF] Partners' Service ECHA Fee calculator [XLS]
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09/11/21
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general
Create the following documents using the available formats as necessary. Document Description Summary of risk management measures (RMMs) and operational conditions (OCs) This document contains...
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14/10/21
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Applications for Authorisation
Format used by ECHA's Committees to write their opinions is provided
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15/09/21
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Applications for Authorisation
Contact list for applicants for authorisation
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17/08/21
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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
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Applications for Authorisation
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25/05/21
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Active substance approval
Follow us Read ECHA Weekly news Subscribe to our news
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08/04/21
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Applications for Authorisation
Related Links Instructions for providing comments Statistics on received applications AfA consultations windows Upcoming consultations on applications for authorisation
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08/04/21
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Applications for Authorisation
The application for authorisation process includes a period of consultation. It lasts for eight weeks. Provide your comments In order to facilitate the work of ECHA's Committees in reviewing the...
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08/04/21
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Applications for Authorisation
All authorisation decisions have a time-limited review period. During this period, authorisation holders have to continue looking for a suitable alternative substance or technology that would make...
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15/03/21
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Applications for Authorisation
This page provides further information on the applications for authorisation or review reports, which have undergone consultation. The applications for authorisation are in the opinion development...
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05/03/21
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Applications for Authorisation
9. Submit a review report if you still need to use the substance If you need to continue using the substance after the review period, you need to submit a review report at least 18 months before...
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01/03/21
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Applications for Authorisation
8. Fulfil your obligations after European Commission's decision Make sure that you fulfil any obligations after the Commission's decision, such as implementing conditions or, if you are a...
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01/03/21
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Applications for Authorisation
7. Engage during the opinion development Follow your application's processing from consultation to the development of the Committees' opinions.
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01/03/21
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Applications for Authorisation
6. Submit your application Submit your application in one of the submission windows.
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01/03/21
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Applications for Authorisation
5. Finalise your application Finalise the reports and prepare everything you need for submission.
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01/03/21
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Applications for Authorisation
4. Notify ECHA and request a Teleconference based information session (TIS) Let ECHA know of your intention to submit in advance and request a Teleconference based information session (TIS) to ask...
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01/03/21
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Applications for Authorisation
3. Start preparing your application Find out what to include in your application and start preparing the necessary reports.
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01/03/21
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Applications for Authorisation
2. Develop an application strategy Communicate with your supply chain and develop a strategy on how best to proceed.
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01/03/21
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Applications for Authorisation
1. Find out whether you are affected by authorisation Check whether your substance is on the Authorisation List and whether any exemptions apply to your uses.
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01/03/21
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Applications for Authorisation
CSR, AoA, SP and SEA
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26/02/21
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Applications for Authorisation
CSR, AoA and SEA
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26/02/21
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Applications for Authorisation
CSR, AoA, SP and SEA *
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26/02/21
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Applications for Authorisation
Adequate control not demonstrated and no suitable alternatives available in the EU
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26/02/21
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Applications for Authorisation
Adequate control demonstrated and suitable alternatives available in the EU
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26/02/21
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Applications for Authorisation
CSR, AoA and SEA *
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26/02/21
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Applications for Authorisation
Adequate control not demonstrated and suitable alternatives available in the EU - but not feasible for the applicant **
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26/02/21
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Applications for Authorisation
*Not mandatory but highly recommended **Authorisation cannot be granted if the alternatives are feasible for the applicant
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26/02/21
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Applications for Authorisation
4. Notify ECHA and request a teleconference-based information session
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26/02/21
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