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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
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19/01/21
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19/01/21
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15/01/21
Comments on the substitution plan Comments on the substitution plan afa_sp_comments_moca_reachlaw_en.docx (267 KBk)
Comments on the substitution plan
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30/11/20
Comments on the substitution plan Comments on the substitution plan afa_sp_comments_ct_reachlaw_en.docx (363 KBk)
Comments on the substitution plan
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30/11/20
Comments on the substitution plan Comments on the substitution plan afa_sp_comments_ct_hapoc_en.docx (2.1 MBk)
Comments on the substitution plan
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30/11/20
Comments on the substitution plan Comments on the substitution plan afa_sp_comments_ct_chemservice_en.docx (951 KBk)
Comments on the substitution plan
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30/11/20
Identification of SVHCs (more) Recommendation for inclusion in the Authorisation List (more) Applications for authorisation (more) Purpose To identify which substances will be included in the...
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17/11/20
Please read carefully the following terms and conditions of echa webforms for the purpose of notifying an intention to submit an application for authorisation and for requesting a teleconference...
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10/11/20
Succinct summary of representative risk management measures (RMMs) and operational conditions (OCs) Succinct summary of representative risk management measures (RMMs) and operational conditions (OCs) afa_ope_siemens_2_rmm_use4_5_public_update_en.pdf (221 KBk)
Succinct summary of representative risk management measures (RMMs) and operational conditions (OCs)
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28/10/20
Succinct summary of representative risk management measures (RMMs) and operational conditions (OCs) Succinct summary of representative risk management measures (RMMs) and operational conditions (OCs) afa_ope_siemens_2_rmm_use1_2_3_public_update_en.pdf (270 KBk)
Succinct summary of representative risk management measures (RMMs) and operational conditions (OCs)
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28/10/20
Chemical safety report
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28/10/20
Chemical safety report
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28/10/20
Responses to RAC and SEAC requests by Applicant(s) (non confidential) Responses to RAC and SEAC requests by Applicant(s) (non confidential) afa_ope-154-info_requests_en.pdf (680 KBk)
Responses to RAC and SEAC requests by Applicant(s) (non confidential)
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15/10/20
Responses to RAC and SEAC requests by Applicant(s) (non confidential) Responses to RAC and SEAC requests by Applicant(s) (non confidential) afa_ope-171-info_requests_en.zip (2.6 MBk)
Responses to RAC and SEAC requests by Applicant(s) (non confidential)
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15/10/20
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09/06/20
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09/06/20
Application for Authorisation - Template Substitution Plan Application for Authorisation - Template Substitution Plan substitution_plan_template_en.rtf (261 KBk)
Application for Authorisation - Template Substitution Plan
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29/05/20
Application for Authorisation - Template for substitution plan Application for Authorisation - Template for substitution plan sub_plan_template_en.pdf (97 KBk)
Application for Authorisation - Template for substitution plan
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29/05/20