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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
../file-system/small/txt ../file-system/small/txt TIS - Legal notice
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
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
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
Status of pre-submission activities and received applications for authorisation per year.
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12/11/19
Status of received review reports per substance:
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12/11/19
Status of received applications for authorisation per substance.
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12/11/19
Status of received review reports per year.
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12/11/19
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27/06/19
../file-system/small/txt ../file-system/small/txt Authorisation - tabs
Substances of very high concern identification Recommendation for the Authorisation List Applications for authorisation
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11/06/19
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
8. Fulfil your obligations after European Commission's decision
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05/03/19
7. Engage during the opinion development
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05/03/19
6. Submit your application
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05/03/19
5. Finalise your application
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05/03/19
3. Start preparing your application
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05/03/19
2. Develop an application strategy
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05/03/19
Format for
analysis of alternatives
and
socio-economic analysis
with instructions Format for analysis of alternatives and socio-economic analysis with instructions aoa_sea_format_without_instructions_2014_en.doc (116 KBk)
Format for analysis of alternatives and socio-economic analysis with instructions
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12/02/19
Format for analysis of alternatives and socio-economic analysis Format for analysis of alternatives and socio-economic analysis aoa_sea_format_annotated_2017_en.doc (190 KBk)
Format for analysis of alternatives and socio-economic analysis
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12/02/19
Template for Socio-economic analysis Template for Socio-economic analysis socioecon_template_2017_en.rtf (49 KBk)
Template for Socio-economic analysis
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12/02/19
Template  for socioeconomic analysis Template for socioeconomic analysis socio_economic_analysis_template_2017__en.pdf (506 KBk)
Template for socioeconomic analysis
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12/02/19
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12/02/19
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11/02/19
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
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
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
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
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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06/11/18
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
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
../file-system/small/txt ../file-system/small/txt REACH - link to consumerssite
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