Registration
Rekisteröintiä koskevat toimintaohjeet
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01/02/22
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Registration
Registreerimisjuhend
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01/02/22
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Registration
Orientaciones sobre el registro
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01/02/22
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Registration
Καθοδήγηση σχετικά με την καταχώριση
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01/02/22
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general
Support ECHA Accounts manual for Industry Users Guidance on registration How to act in dossier or substance evaluation How to cease manufacture How to report changes in identity under REACH and CLP
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14/12/21
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general
Support Creating your registration dossier How to prepare registration and PPORD dossiers Guidance on registration Submitting your registration dossier What information you need
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14/12/21
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general
Support Guidance on registration
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14/12/21
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general
See also under the Legislation section Evaluation Registration
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14/12/21
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general
Support Dossier evaluation decisions Guidance on registration Substance evaluation decisions
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13/12/21
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general
Support Dissemination and Confidentiality under the REACH Regulation How to prepare an inquiry dossier What information you need
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13/12/21
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general
Support Guidance on registration
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13/12/21
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general
See also under the Legislation section Inquiry
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13/12/21
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general
See also under the Legislation section Evaluation
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13/12/21
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Data sharing
Guidance on Registration
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17/08/21
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general
REACH is a regulation of the European Union, adopted to improve the protection of human health and the environment from the risks that can be posed by chemicals, while enhancing the competitiveness...
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02/08/21
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Active substance approval
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08/04/21
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Registration
Manufacturers, importers and downstream users based in the EU can submit a request for the use of an alternative chemical name to ECHA. It is not possible to appoint a ‘Third Party Representative’...
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08/03/21
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../file-system/small/txt
PPORD
Registration
If your substance is subject to product and process orientated research and development (PPORD), you can submit a PPORD notification to ECHA in order to be exempted from the obligation to register.
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04/03/21
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Registration
See also under the Support section Registration Questions and Answers on Registration
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25/02/21
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Dossier evaluation
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
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Dossier evaluation
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
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Dossier evaluation
Classification and labelling
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22/02/21
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Dossier evaluation
Adaptations
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22/02/21
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Dossier evaluation
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
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Registration
As a registrant of a substance, you need to compile all the required information in a registration dossier, which has two main components: A technical dossier is always required for all substances...
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10/06/20
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Registration
If you have prepared your registration dossier in IUCLID, you need to submit it to ECHA through REACH-IT. REACH-IT is the central IT system for companies to securely submit, process and manage...
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10/06/20
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Registration
There are four steps in the process of data gathering before registering a substance. Agree with your co-registrants how to divide the work or whether to outsource some, or all of it. 1. Collect...
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10/06/20
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Registration
Typically, tests are contracted out as a package. This has the advantage of being performed by experts in the most time-efficient manner and according to the required quality standards and legal...
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10/06/20
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Registration
A test performed in vitro ("in the glass") means that it is done outside of a living organism and it usually involves isolated tissues, organs or cells. You can use in vitro data to fully or partly...
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10/06/20
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Registration
If you manufacture or import a substance in amounts less than one tonne a year, you do not need to register the substance. If you reach or exceed this threshold, your tonnage band will determine...
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10/06/20
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Registration
To register a substance in the 10 to 100 tonnage band, you need to provide information specified in Column 1 of REACH Annexes VII and VIII, comprising certain physicochemical data, toxicological...
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10/06/20
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Registration
To register a substance in the 1 to 10 tonnage band, you need to provide information specified in Column 1 of REACH Annex VII, including certain physicochemical data, toxicological information and...
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10/06/20
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Registration
If you only have a few substances to manage, you can take advantage of the IUCLID Cloud to create your dossiers in the IUCLID format. To use the service, you will need an ECHA account and to...
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10/06/20
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Registration
Under REACH, testing on vertebrate animals (e.g. rats, other mammals or fish) can only be used as a last resort to fulfil information requirements for registration. There are multiple ways to avoid...
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10/06/20
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Registration
ECHA assigns a submission number to each received dossier. This number is used as a reference in all correspondence relating to this registration until a registration number is assigned. Dossier...
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10/06/20
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Registration
You will need to share data and register your substance jointly with other companies. In practice, this means that you need to: Submit an inquiry via REACH-IT to ask ECHA if you have...
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10/06/20
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Registration
Claiming an “adaptation” means that it is possible to omit a test based on certain general rules or specific rules that apply for just one information requirement. General rules for adaptations can...
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10/06/20
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Registration
In your registration dossier you also have to report / provide information on how your substance is used in your supply chain. To retrieve such information you can use many sources, for example:...
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10/06/20
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Registration
Demonstrating the safe use of your substance in a registration dossier requires a significant investment of time, money and expertise. You will need to have dialogue and, normally, contractual...
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10/06/20
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Registration
Once you know the identity of your substance, you need to see if your substance needs to be registered or if it is exempt from registration. On ECHA’s website you can check if your substance is...
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10/06/20
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Registration
You need to determine whether it is you who needs to register a substance or another actor in your supply chain.
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10/06/20
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Registration
Questions and Answers Pre-registration Inquiry Registration Joint submission NONS
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20/04/20
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Registration
These Dos and Don'ts can help make negotiations successful. Dos Don'ts Before the negotiations ✓ Establish and maintain clear contact details, if possible a functional electronic mailbox to...
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12/03/20
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Registration
IUCLID is a software to record, store, maintain and exchange data on intrinsic and hazard properties of chemical substances. ECHA co-develops the software with the OECD. Under REACH, information...
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12/03/20
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Registration
See also under the Legislation section Registration
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11/03/20
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Registration
See also under the Legislation section Registration
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06/03/20
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Registration
The following elements must be part of the data-sharing agreement: Data itemisation The existing registrant must provide information on the specific data to be shared. This information must allow...
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06/03/20
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Registration
REACH requires existing registrants and potential registrants to make every effort to reach an agreement on sharing data. The legislation also requires that the costs of sharing the information for...
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06/03/20
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Registration
Support Sector-specific support for substance identification Guidance on substance identification How to characterise and identify your substance Getting started with EU chemicals legislation...
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26/02/20
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Registration
See also under the Legislation section Substance identification
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26/02/20
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