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Comments submitted to date Comments submitted to date afa_comments_0222-01_en.zip (4 MBk)
Comments submitted to date
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14/01/22
Related Substitution to safer chemicals Authorisation supply chain coverage [PDF] Partners' Service ECHA Fee calculator [XLS]
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09/11/21
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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27/10/21
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
../file-system/small/txt ../file-system/small/txt Status of received notifications
30 September 2021 Downstream uses notified (active) Uses for which own authorisation is held*) Total authorised uses Bis(2-ethylhexyl)phthalate (DEHP) 8 2 10 Chromium trioxide 1457 98 1555 Dibutyl...
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11/10/21
../file-system/small/txt ../file-system/small/txt DU 66 notification intro & bg
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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08/10/21
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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05/10/21
Format used by ECHA's Committees to write their opinions is provided Format used by ECHA's Committees to write their opinions is provided format_rac_seac_opinions_en.pdf (363 KBk)
Format used by ECHA's Committees to write their opinions is provided
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15/09/21
../file-system/small/txt ../file-system/small/txt Afa consultations related links
Related links Comitology register European Commission: Authorisation decisions Downstream uses covered by granted authorisations Status of Authorisation decisions [XLSX] (updated 30/6/2021)
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14/09/21
Contact list for applicants for authorisation Contact list for applicants for authorisation afa_contact_list_en.xlsx (55 KBk)
Contact list for applicants for authorisation
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17/08/21
../file-system/small/txt ../file-system/small/txt Legislation - REACH Regulation
REACH Legislation
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09/06/21
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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04/06/21
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25/05/21
../file-system/small/txt ../file-system/small/txt Homepage subscribe
Follow us Read ECHA Weekly news Subscribe to our news
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22/04/21
../file-system/small/txt ../file-system/small/txt AfA - see also
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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15/04/21
../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
../file-system/small/txt ../file-system/small/txt Related Links
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
../file-system/small/txt ../file-system/small/txt applications for authorisation 2
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
../file-system/small/txt ../file-system/small/txt How to submit a review report
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
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
../file-system/small/txt ../file-system/small/txt Submit a review report
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
../file-system/small/txt ../file-system/small/txt Applying for authorisation step 8
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
../file-system/small/txt ../file-system/small/txt Applying for authorisation step 7
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
../file-system/small/txt ../file-system/small/txt Applying for authorisation step 6
6. Submit your application Submit your application in one of the submission windows.
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01/03/21
../file-system/small/txt ../file-system/small/txt Applying for authorisation step 5
5. Finalise your application Finalise the reports and prepare everything you need for submission.
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01/03/21
../file-system/small/txt ../file-system/small/txt Applying for authorisation step 4
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
../file-system/small/txt ../file-system/small/txt Applying for authorisation step 3
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
../file-system/small/txt ../file-system/small/txt Applying for authorisation step 2
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
../file-system/small/txt ../file-system/small/txt Applying for authorisation step 1
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
CSR, AoA, SP and SEA
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26/02/21
CSR, AoA and SEA
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26/02/21
CSR, AoA, SP and SEA *
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26/02/21
Adequate control not demonstrated and no suitable alternatives available in the EU
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26/02/21
Adequate control demonstrated and suitable alternatives available in the EU
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26/02/21
CSR, AoA and SEA *
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26/02/21
Adequate control not demonstrated and suitable alternatives available in the EU - but not feasible for the applicant **
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26/02/21
*Not mandatory but highly recommended **Authorisation cannot be granted if the alternatives are feasible for the applicant
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26/02/21
4. Notify ECHA and request a teleconference-based information session
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26/02/21
There are two possible procedures under which an authorisation to use an Annex XIV substance may be granted: Adequate control route: by demonstrating that the risk from using the substance is...
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26/02/21
Adequate control demonstrated and no suitable alternatives available in the EU
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26/02/21
../file-system/small/txt ../file-system/small/txt Start preparing your application
The preparation of these reports requires a substantial amount of data (e.g. on conditions of use, potential alternatives to using the substance and socio-economic information), which may only be...
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26/02/21
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09/02/21
Compiled RAC and SEAC opinions Compiled RAC and SEAC opinions afa_ope-0203-01-fo_en.pdf (446 KBk)
Compiled RAC and SEAC opinions
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20/01/21
Compiled RAC and SEAC opinions Compiled RAC and SEAC opinions afa_ope-0203-02-fo_en.pdf (495 KBk)
Compiled RAC and SEAC opinions
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20/01/21
Compiled RAC and SEAC opinions Compiled RAC and SEAC opinions afa_npe-0207-01-fo_en.pdf (408 KBk)
Compiled RAC and SEAC opinions
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20/01/21
Compiled RAC and SEAC opinions Compiled RAC and SEAC opinions afa_npe-0207-02-fo_en.pdf (470 KBk)
Compiled RAC and SEAC opinions
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20/01/21
Comments submitted to date Comments submitted to date afa_comments_0219-01_en.zip (6.8 MBk)
Comments submitted to date
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19/01/21
Comments submitted to date Comments submitted to date afa_comments_0224-01_en.zip (92 KBk)
Comments submitted to date
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19/01/21
Comments submitted to date Comments submitted to date afa_comments_0223-01_en.zip (73 KBk)
Comments submitted to date
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19/01/21
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19/01/21