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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
Related Authorisation process Addressing substances of concern Registry of SVHC Intentions Candidate list of SVHCs Candidate List obligations Consultation for the identification of substances of...
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23/04/20
The consultation starts when ECHA publishes the broad information on uses applied for on its website, inviting interested parties to submit information on possible alternative substances or...
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31/03/20
../file-system/small/txt ../file-system/small/txt Authorisation
The authorisation procedure aims to assure that the risks from Substances of Very High Concern are properly controlled and that these substances are progressively replaced by suitable alternatives...
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31/03/20
../file-system/small/txt ../file-system/small/txt Afa - Adopted opinions
Past consultations and opinions The page contains the applications, the comments received during the consultations and the applicants' responses. More
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31/03/20
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18/03/20
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18/03/20
Step 6. Pay the invoice by the date mentioned in it.
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30/01/20
Step 4. If you are part of a joint application, follow the steps in the graph below. If you are not part of a joint application, skip this step and go directly to point 5. A detailed description of...
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30/01/20
Step 2. Create your IUCLID dossier. Follow the instructions in the manual.
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30/01/20
Step 5. Finalise the broad information on uses. After you have passed the business rules check and before the invoice is sent, ECHA will review the proposed 'brief wording' on the broad information...
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30/01/20
Step 3. Submit your application through REACH-IT. Follow the instructions in the manual. For joint applications, follow the instructions in step 4. Send your application during the first days of...
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30/01/20
Step 1. Create your account in REACH-IT if you do not have one. If you already have an account, ensure that all information is up-to-date. Note that ECHA will use the company size stated in your...
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30/01/20
../file-system/small/txt ../file-system/small/txt submit joint AfA
<svg id="Layer_1" data-name="Layer1" xmlns="http://www.w3.org/2000/svg" xmlns:xlink="http://www.w3.org/1999/xlink" viewBox="0 0 615.11 392.11" width=513...
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30/01/20
SME verification The application for authorisation process follows the same SME verification conditions as the REACH registration process. If you claim to be eligible for a fee reduction, ECHA will...
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30/01/20
Business rules check, latest application date and invoice The business rules check aims to ensure that your application fulfils a set of administrative pre-requisites. Your application needs to...
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30/01/20
Further information Consultation on applications for authorisation
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16/01/20
../file-system/small/txt ../file-system/small/txt Applications for authorisation
Manufacturers, importers or downstream users can apply for an authorisation for the placing on the market or the use of a substance on the Authorisation List.
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16/01/20
Identification of SVHCs During the consultation for the identification of an SVHC, ECHA particularly welcomes comments related to the substance identity (i.e. on the substance name/EC number/CAS...
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09/01/20
The authorisation process aims to ensure that substances of very high concern (SVHCs) are progressively replaced by less dangerous substances or technologies where technically and economically...
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09/01/20