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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Applications for Authorisation
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
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Applications for Authorisation
Adequate control demonstrated and no suitable alternatives available in the EU
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26/02/21
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Applications for Authorisation
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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Applications for Authorisation
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09/02/21
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Applications for Authorisation
Compiled RAC and SEAC opinions
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20/01/21
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Applications for Authorisation
Compiled RAC and SEAC opinions
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20/01/21
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Applications for Authorisation
Compiled RAC and SEAC opinions
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20/01/21
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Applications for Authorisation
Compiled RAC and SEAC opinions
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20/01/21
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Applications for Authorisation
Comments submitted to date
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19/01/21
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Applications for Authorisation
Comments submitted to date
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19/01/21
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Applications for Authorisation
Comments submitted to date
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19/01/21
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Applications for Authorisation
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19/01/21
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Applications for Authorisation
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19/01/21
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Applications for Authorisation
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19/01/21
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Applications for Authorisation
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15/01/21
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Applications for Authorisation
Comments on the substitution plan
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30/11/20
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Applications for Authorisation
Comments on the substitution plan
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30/11/20
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Applications for Authorisation
Comments on the substitution plan
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30/11/20
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Applications for Authorisation
Comments on the substitution plan
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30/11/20
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Recommendation for inclusion in the Authorisation List
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
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Applications for Authorisation
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
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Applications for Authorisation
Succinct summary of representative risk management measures (RMMs) and operational conditions (OCs)
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28/10/20
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Applications for Authorisation
Succinct summary of representative risk management measures (RMMs) and operational conditions (OCs)
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28/10/20
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Applications for Authorisation
Chemical safety report
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28/10/20
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Applications for Authorisation
Chemical safety report
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28/10/20
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Applications for Authorisation
Responses to RAC and SEAC requests by Applicant(s) (non confidential)
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15/10/20
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Applications for Authorisation
Responses to RAC and SEAC requests by Applicant(s) (non confidential)
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15/10/20
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Applications for Authorisation
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09/06/20
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Applications for Authorisation
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09/06/20
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Applications for Authorisation
Application for Authorisation - Template Substitution Plan
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29/05/20
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Applications for Authorisation
Application for Authorisation - Template for substitution plan
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29/05/20
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