| 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...  Similar Results | 08/03/21 |
| Registration Summary 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... Similar Results | 04/03/21 |
| Dossier evaluation Registration To meet your registration obligations, you must fulfil the minimum standard information requirements set by REACH. These requirements depend on the volume of the substance you... Similar Results | 04/03/21 |
| Registration How to prepare registration and PPORD dossiers October 2020 How to prepare registration and PPORD dossiers Release date October 2020 2 ... Similar Results | 03/03/21 |
| Jobs Registration 22 February 2021 1 Information on manual verification at completeness check ECHA performs a completeness check on each incoming registration to ensure that... Similar Results | 01/03/21 |
| Registration See also under the Support section Registration Questions and Answers on Registration Similar Results | 25/02/21 |
| Dossier evaluation Substance evaluation Registration Related Substance evaluation – CoRAP table Substance evaluation Evaluation process Practical guide on how to act in substance evaluation Community rolling action plan Similar Results | 22/02/21 |
| Dossier evaluation Registration Related Understanding CLP C&L Inventory How to submit and update your C&L notification Implementing Regulation (EU) 2020/1435 Similar Results | 22/02/21 |
| Dossier evaluation Registration Related Substance identification process under REACH Substance identification – get started Guidance on substance identification How to prepare registrations for nanomaterials... Similar Results | 22/02/21 |
| Dossier evaluation Registration Related Public activities coordination tool Substances of potential concern Examination of testing proposals Strategy for gathering your data Adaptations Good Laboratory... Similar Results | 22/02/21 |
| Dossier evaluation Registration Classification and labelling Similar Results | 22/02/21 |
| Dossier evaluation 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... Similar Results | 22/02/21 |
| Dossier evaluation Registration 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... Similar Results | 22/02/21 |
| Dossier evaluation Registration 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... Similar Results | 22/02/21 |
| Dossier evaluation Registration 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... Similar Results | 22/02/21 |
| Registration Substance evaluation Restriction Applications for Authorisation REACH Regulation Consolidated version of the REACH Regulation The consolidated version of the Regulation (EC) No 1907/2006 of the European Parliament and of the Council on the... Similar Results | 08/02/21 |
| Registration Please note that Annex III has been modified by Regulation 2018/1881, modifying provisions in case of nanomaterials (Commission Regulation (EU) 2018/1881 of 3 December 2018... Similar Results | 08/02/21 |
| Registration Please note: The REACH Registered substance portal was updated on 9th November 2020; the REACH registered factsheets were further updated on 21st December 2020. Details of the... Similar Results | 18/01/21 |
| Registration How to prepare an inquiry dossier October 2020 How to prepare an inquiry dossier Release date October 2020 2 P.O. Box 400,... Similar Results | 28/10/20 |
| Registration Dissemination and Confidentiality under the REACH Regulation Release date October 2020 1 P.O. Box 400, FI-00121 Helsinki, Finland | Tel. +358 9 686180 | echa.europa.eu ... Similar Results | 28/10/20 |
| 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... Similar Results | 10/06/20 |
| 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,... Similar Results | 10/06/20 |
| 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... Similar Results | 10/06/20 |
| 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... Similar Results | 10/06/20 |
| 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... Similar Results | 10/06/20 |
| Registration The registration dossier has to reflect the current knowledge on how your substance can be used safely at production sites and by users throughout the supply chain. This... Similar Results | 10/06/20 |
| 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... Similar Results | 10/06/20 |
| 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... Similar Results | 10/06/20 |
| 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,... Similar Results | 10/06/20 |
| 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... Similar Results | 10/06/20 |
| 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... Similar Results | 10/06/20 |
| Registration Your dossier will go through the following steps after submission: 1. Business rules check The business rules check makes sure that your dossier can be processed by ECHA. For... Similar Results | 10/06/20 |
| 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... Similar Results | 10/06/20 |
| 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... Similar Results | 10/06/20 |
| 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... Similar Results | 10/06/20 |
| Registration After you have compiled all the information on your substance necessary for fulfilling the REACH requirements, you need to document your findings in a registration dossier. The... Similar Results | 10/06/20 |
| Registration The minimum data requirements for registration of your substance are specified in Annexes VI - X of REACH. The legal requirements (standard information requirements) are... Similar Results | 10/06/20 |
| 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,... Similar Results | 10/06/20 |
| 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... Similar Results | 10/06/20 |
| Registration You need to determine whether it is you who needs to register a substance or another actor in your supply chain. 1. What is your identity as a registrant? You can only... Similar Results | 10/06/20 |
| Registration In a registration you show that the substance you deal with is handled safely throughout the supply chain, ensuring that human health and the environment are protected. You... Similar Results | 10/06/20 |
| Registration Substance evaluation Restriction Applications for Authorisation 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... Similar Results | 03/06/20 |
| Registration Questions and Answers Pre-registration Inquiry Registration Joint submission NONS Similar Results | 20/04/20 |
| 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... Similar Results | 12/03/20 |
| 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... Similar Results | 12/03/20 |
| Registration SME See also under the Legislation section Registration Similar Results | 11/03/20 |
| Registration See also under the Legislation section Registration Similar Results | 06/03/20 |
| 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... Similar Results | 06/03/20 |
| 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... Similar Results | 06/03/20 |
| Registration Related Guidance on information requirements and chemical safety assessment, R.6 QSAR and grouping of chemicals The Read-across assessment framework [PDF] [EN] Human health:... Similar Results | 18/02/20 |
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