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Rekisteröintiä koskevat toimintaohjeet Rekisteröintiä koskevat toimintaohjeet registration_fi.pdf (1.1 MBk)
Rekisteröintiä koskevat toimintaohjeet
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01/02/22
Registreerimisjuhend Registreerimisjuhend registration_et.pdf (1 MBk)
Registreerimisjuhend
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01/02/22
Orientaciones sobre el registro Orientaciones sobre el registro registration_es.pdf (1.2 MBk)
Orientaciones sobre el registro
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01/02/22
Καθοδήγηση σχετικά με την καταχώριση Καθοδήγηση σχετικά με την καταχώριση registration_el.pdf (1.4 MBk)
Καθοδήγηση σχετικά με την καταχώριση
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01/02/22
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
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
Support Guidance on registration
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14/12/21
See also under the Legislation section Evaluation Registration
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14/12/21
Support Dossier evaluation decisions Guidance on registration Substance evaluation decisions
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13/12/21
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
Support Guidance on registration
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13/12/21
See also under the Legislation section Inquiry
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13/12/21
See also under the Legislation section Evaluation
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13/12/21
Guidance on Registration Guidance on Registration registration_en.pdf (1.4 MBk)
Guidance on Registration
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17/08/21
../file-system/small/txt ../file-system/small/txt Understanding REACH
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
../file-system/small/txt ../file-system/small/txt Content pages - Subscribe
Follow us Read ECHA Weekly news Subscribe to our news
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08/04/21
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
../file-system/small/txt ../file-system/small/txt PPORD
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
../file-system/small/txt ../file-system/small/txt Registration - support
See also under the Support section Registration Questions and Answers on Registration
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25/02/21
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 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
../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
../file-system/small/txt ../file-system/small/txt What information you need to submit
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
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
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
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
../file-system/small/txt ../file-system/small/txt In vitro methods main
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
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
../file-system/small/txt ../file-system/small/txt inforeq 10 to 100 main
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
../file-system/small/txt ../file-system/small/txt inforeq 1 to 10 tonnes main
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
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
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
../file-system/small/txt ../file-system/small/txt From submission to decision
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
../file-system/small/txt ../file-system/small/txt Finding your co-registrants
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
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
../file-system/small/txt ../file-system/small/txt Collecting information on uses main
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
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
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
../file-system/small/txt ../file-system/small/txt Do I need to register?
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
Questions and Answers Pre-registration Inquiry Registration Joint submission NONS
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20/04/20
../file-system/small/txt ../file-system/small/txt dos and dont's table
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
../file-system/small/txt ../file-system/small/txt What is IUCLID
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
../file-system/small/txt ../file-system/small/txt SMEs and consultants:See also
See also under the Legislation section Registration
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11/03/20
See also under the Legislation section Registration
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06/03/20
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
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
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
See also under the Legislation section Substance identification
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26/02/20