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Related Information requirements Practical guide for SME managers and REACH coordinators - How to fulfil your information requirements at tonnages 1-10 and 10-100 tonnes per year Guidance on...
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21/12/21
Guidance on Registration Guidance on Registration registration_en.pdf (1.4 MBk)
Guidance on Registration
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17/08/21
Related Substance evaluation – CoRAP table Substance evaluation Evaluation process Practical guide on how to act in substance evaluation Community rolling action plan
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22/02/21
Related Understanding CLP C&L Inventory How to submit and update your C&L notification Implementing Regulation (EU) 2020/1435
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22/02/21
Related Substance identification process under REACH Substance identification – get started Guidance on substance identification How to prepare registrations for nanomaterials [PDF]
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22/02/21
Related Public activities coordination tool Substances of potential concern Examination of testing proposals Strategy for gathering your data Adaptations Good Laboratory Practice Dossier evaluation...
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22/02/21
../file-system/small/txt ../file-system/small/txt Recommendations - cnl box
Classification and labelling
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22/02/21
../file-system/small/txt ../file-system/small/txt Recommendations - adaptions box
Adaptations
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22/02/21
Keep your registrations up to date and take actions to proactively improve your registration data by following these general recommendations. Monitor changes and update by relevant deadlines You...
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22/02/21
../file-system/small/txt ../file-system/small/txt Recommendations - substance id
Companies need to clearly identify the substances they manufacture or import. This makes it possible for companies to register the same substance jointly, following the ‘one substance, one...
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22/02/21
../file-system/small/txt ../file-system/small/txt Recommendations - registration
If your company manufactures or imports substances in quantities of more than one tonne per year, you are responsible for compiling and submitting a registration dossier to ECHA. The following...
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22/02/21
You need to carry out exposure assessment and risk characterisation for substances registered at or above 10 tonnes per year, if they are classified as dangerous or as having persistent,...
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22/02/21
In dossier evaluation, ECHA checks if the information that you have submitted in your registration meets the requirements set in REACH for your substance and tonnage band. If your dossier does not...
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22/02/21
../file-system/small/txt ../file-system/small/txt Recommendations - cnl
Classification and labelling is the starting point for hazard communication and important elements in making sure that human health and the environment are protected from harmful chemicals....
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22/02/21
../file-system/small/txt ../file-system/small/txt Recommendations - adaptions panels
An adaptation to a standard information requirement means that instead of performing a test, you provide a justification. Your justification has to either be based on general rules as explained in...
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22/02/21
Substance evaluation is carried out by the EU Member States. It aims to clarify potential risks related to the safe use of a substance. The evaluating competent authority may request information...
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22/02/21
../file-system/small/txt ../file-system/small/txt Recommendations - introduction
All REACH registrants must proactively review and update the information in their registration dossiers and are encouraged to improve the quality and relevance of the included data. The following...
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01/02/21
Related Practical Guide on How to act in dossier evaluation Evaluation process Dossier evaluation status
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21/02/20
../file-system/small/txt ../file-system/small/txt CoRAP status - need help
See a problem or have feedback?
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30/01/20
../file-system/small/txt ../file-system/small/txt Evaluation process
Phases OVERVIEW Evaluation process PHASE 1 Assessment PHASE 2 Decision making PHASE 3 Follow-up to ECHA’s decision REACH aims to protect human health and the environment, and its evaluation process...
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13/01/20
../file-system/small/txt ../file-system/small/txt Evaluation
ECHA and the Member States evaluate the information submitted by companies to examine the quality of the registration dossiers and the testing proposals and to clarify if a given substance...
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25/11/19
../file-system/small/txt ../file-system/small/txt Evaluation Process: Actors
Evaluation Process: Actors
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14/11/19
../file-system/small/txt ../file-system/small/txt Evaluation - Links
Related Guidance on REACH Practical guides Questions and answers REACH Legislation
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30/10/19
../file-system/small/txt ../file-system/small/txt Registrant: related links
Related Registrant Registration under REACH Guidance on Information Requirements and Chemical Safety Assessment Practical guides: How to act in dossier evaluation and How to act in substance...
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25/09/19
Standard information requirements
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23/05/19
../file-system/small/txt ../file-system/small/txt Recommendations - registration box
Registration
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23/05/19
../file-system/small/txt ../file-system/small/txt Recommendations - substance id box
Substance identification
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23/05/19
../file-system/small/txt ../file-system/small/txt Recommendations - general box
General recommendations
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23/05/19
../file-system/small/txt ../file-system/small/txt Recommendations - exposure box
Exposure assessment and risk characterisation
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23/05/19
../file-system/small/txt ../file-system/small/txt Evaluation progress reports - text
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27/02/19
Related Guidance on chemical safety assessment (including parts B and D) Chemical safety report EScom standard (Cefic) Sector use map formats
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05/11/18
../file-system/small/txt ../file-system/small/txt Recommendations - adaptions related
Related Adaptations How to avoid animal testing Practical guide on how to use and report QSARs Grouping of substances and read-across
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05/11/18
Related Registration process How to register Practical guide on how to assess whether a substances is used as an intermediate under strictly controlled conditions
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05/11/18
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30/10/18
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30/10/18
How to read the table ECHA’s information systems automatically update the status of dossier evaluations during the process. For transparency reasons, all dossier evaluation decisions will remain...
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08/10/18
Content of the table Identifiers of the substance: Name (as on the Dissemination website); EC/List number (European Community number / List number assigned by ECHA); CAS number (also called the...
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08/10/18
../file-system/small/txt ../file-system/small/txt Evaluation decisions
ECHA’s dossier evaluation process covers compliance checks and the examination of testing proposals. By consulting the table below, you can find out whether ECHA has started to evaluate dossiers...
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05/10/18
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03/05/18
Further information Evaluation Process Dossier Compliance Checks Testing Proposals examination Testing Proposals consultation
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18/11/14
Evaluation process graph Evaluation process graph evaluation_process_big_en.pdf (3.5 MBk)
Evaluation process graph
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26/02/13
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21/02/13
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11/09/12
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11/09/12
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11/09/12