Recommendation for inclusion in the Authorisation List
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
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Applications for Authorisation
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
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Recommendation for inclusion in the Authorisation List
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
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Applications for Authorisation
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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Applications for Authorisation
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18/03/20
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Applications for Authorisation
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18/03/20
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Applications for Authorisation
Step 6. Pay the invoice by the date mentioned in it.
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30/01/20
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Applications for Authorisation
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
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Applications for Authorisation
Step 2. Create your IUCLID dossier. Follow the instructions in the manual.
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30/01/20
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Applications for Authorisation
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
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Applications for Authorisation
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
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Applications for Authorisation
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
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Applications for Authorisation
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30/01/20
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Applications for Authorisation
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
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Applications for Authorisation
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
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Applications for Authorisation
Further information Consultation on applications for authorisation
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16/01/20
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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
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Recommendation for inclusion in the Authorisation List
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
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Recommendation for inclusion in the Authorisation List
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
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Applications for Authorisation
Legal notice ECHA will not be responsible for ensuring that the issues have been understood by the requester. ECHA cannot be held liable for any negative consequences this has on the handling of...
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08/01/20
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Applications for Authorisation
Notify ECHA well in advance (i.e. 8 months) of the date you intend to submit an application for authorisation so that ECHA can ensure a proper resource planning and a smooth processing of all...
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08/01/20
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Applications for Authorisation
Related How to submit a joint application for authorisation in REACH-IT [PDF] [EN] Submission windows Manual: How to prepare an application for authorisation
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16/12/19
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Applications for Authorisation
Status of pre-submission activities and received applications for authorisation per year.
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12/11/19
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Applications for Authorisation
Status of received review reports per substance:
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12/11/19
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Applications for Authorisation
Status of received applications for authorisation per substance.
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12/11/19
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Applications for Authorisation
Status of received review reports per year.
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12/11/19
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Downstream user
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27/06/19
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Recommendation for inclusion in the Authorisation List
Substances of very high concern identification Recommendation for the Authorisation List Applications for authorisation
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11/06/19
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Applications for Authorisation
Essential links Submitting a downstream user notification of authorised uses Format for reporting of occupational exposure data by downstream users [XLSX]
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27/03/19
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Applications for Authorisation
8. Fulfil your obligations after European Commission's decision
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05/03/19
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Applications for Authorisation
7. Engage during the opinion development
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05/03/19
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Applications for Authorisation
6. Submit your application
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05/03/19
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Applications for Authorisation
5. Finalise your application
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05/03/19
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Applications for Authorisation
3. Start preparing your application
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05/03/19
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Applications for Authorisation
2. Develop an application strategy
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05/03/19
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Applications for Authorisation
Format for
analysis of alternatives
and
socio-economic analysis
with instructions
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12/02/19
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Applications for Authorisation
Format for analysis of alternatives and socio-economic analysis
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12/02/19
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Applications for Authorisation
Template for Socio-economic analysis
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12/02/19
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Applications for Authorisation
Template for socioeconomic analysis
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12/02/19
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Applications for Authorisation
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12/02/19
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Applications for Authorisation
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11/02/19
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Applications for Authorisation
If you have a strong case, demonstrate this by being transparent and avoiding unnecessary confidentiality claims in the public versions of the reports. You will need to provide justification for...
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08/02/19
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Applications for Authorisation
The European Commission prepares a draft authorisation decision within three months after receiving the opinions from ECHA. Following the draft decision, a minimum of three months is needed for the...
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30/01/19
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Applications for Authorisation
If any of your substances are affected by authorisation, the next step is to develop a strategy for how to proceed. You should explore whether there are safer alternatives and assess whether it is...
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30/01/19
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Applications for Authorisation
To find out whether your business may be affected by authorisation, you need to have an overview of all your substances and uses. Substances that have been identified as substances of very high...
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30/01/19
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Registration
Further information General Report from the Commission on the operation of REACH and review of certain elements (5 March 2018). Further information related to the ongoing reviews and planned...
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09/11/18
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Applications for Authorisation
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06/11/18
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Applications for Authorisation
Essential links Formats needed to prepare an application Questions & answers Guides and guidance How to apply for authorisation - a step-by-step guide for applicants [PDF] How to develop the...
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01/08/18
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Applications for Authorisation
See also Information from downstream user notifications made public by ECHA Submitting downstream user notification of authorised uses Downstream users: notify ECHA if you use an authorised...
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20/07/18
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Registration
See also under the Chemicals in our Life website How are chemicals controlled Industry to register chemicals Safety precautions and exposure
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30/04/18
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