| Dossier evaluation Registration Under REACH, standard information requirements are those that are required as a minimum to meet your registration obligations, and they depend directly on how much of a...  Similar Results | 31/07/20 |
| Jobs Registration 24 July 2020 1 Information on manual verification at completeness check ECHA performs a completeness check on each incoming registration to ensure that the ... Similar Results | 30/07/20 |
| Registration Webinar related to dossier quality Content Date Substance identity issues covered in the screening campaign Concentration ranges Compositions with no constituents No... Similar Results | 14/07/20 |
| 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 | 14/07/20 |
| 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 Companies are responsible for collecting information on the properties and uses of the substances they manufacture or import above one tonne a year. They also have to assess the... Similar Results | 03/06/20 |
| 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 How to prepare registration and PPORD dossiers How to prepare registration and PPORD dossiers Release date April 2020 2 P.O. Box 400,... Similar Results | 13/05/20 |
| Registration How to prepare an inquiry dossier 2 How to prepare an inquiry dossier Version 5.0 P.O. Box 400, FI-00121 Helsinki, Finland | Tel. +358 9 686180... Similar Results | 04/05/20 |
| 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 The result of the search ‘Substance has nanoform’ returns all factsheets containing data related to nanomaterials. However, this does not mean that a registration covering... Similar Results | 25/02/20 |
| Dossier evaluation Registration REACH requires all registrants to provide sufficient information to identify the substance they manufacture or import. There must be only one registration for each substance, so... Similar Results | 25/02/20 |
| Dossier evaluation Registration Classification and labelling is crucial for ensuring a high level of protection of health and the environment, as well as for the free movement of substances, mixtures and... Similar Results | 24/02/20 |
| Dossier evaluation Substance evaluation Registration Substance evaluation is carried out by the EU Member States. It aims to clarify concerns related to the safe use of a substance. The evaluating competent authority may request... Similar Results | 24/02/20 |
| Dossier evaluation Registration If ECHA considers that your registration dossier is not compliant with the information required for your substance at the tonnage band registered, it will issue a decision. This... Similar Results | 24/02/20 |
| 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 | 24/02/20 |
| Dossier evaluation Registration An adaptation to a standard information requirement means that instead of performing a test, you provide a justification that is either based on general rules or on specific... Similar Results | 21/02/20 |
| 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 |
| Dossier evaluation Registration You are responsible for collecting information on the tonnages, properties and uses of the substances you manufacture or import in quantities of more than one tonne a year. You... Similar Results | 18/02/20 |
| Dossier evaluation Registration These general recommendations highlight ECHA’s key messages for keeping your registration data in order and improving it proactively. Update regularly You are responsible for... Similar Results | 18/02/20 |
| Registration Support Practical examples – REACH registration How to cooperate for REACH registration – best practice for SMEs and consultants Similar Results | 18/02/20 |
| Registration 5 Prepare your registration as a IUCLID dossier How to protect your confidential business information [PDF] These video tutorials highlight different aspects in preparing... Similar Results | 18/02/20 |
| Registration Related Commission Directive (EU) 2019/1831 of 24 October 2019 establishing a fifth list of indicative occupational exposure limit values Commission Directive (EU) 2017/164 of... Similar Results | 08/01/20 |
| Prior Informed Consent Due to IT maintenance activities, some substance tables are temporarily disabled. We will resume the service as soon as possible. ECHA apologises for any inconvenience caused. ... Similar Results | 02/12/19 |
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