Eu reach update

Dossier evaluation focuses on completeness and quality of information. ECHA will notify the registrant of any deficiencies. Chemical substances placed on the CoRAP may eventually be subject to authorization or restriction. The policy objective of this requirement is to ensure adequate control and progressive replacement of these substances. The candidate list identifies the chemical substances the EU is considering imposing an obligation on users to obtain a use-authorization.

Companies that need to apply for authorization may visit the following website for further information: applications for authorization. Importers of articles i. See the guidance on substances in articles for the obligation to notify ECHA and the duty to communicate safe use information.

However, you may not know what chemicals are used in your products. In that case, you will need to gather information about the chemicals in your products first. Contact your suppliers for full-disclosure substance data to ensure you are not receiving any components containing substances that violate REACH. If you cannot access full-disclosure substance data, at least request a non-use SVHC statement.

Suppliers should notify you when SVHC concentration exceeds 0. However, the reality of the situation is your company remains at risk if it relies on its suppliers for notification. Necessary documentation is essential, as companies are required to submit registered dossiers to the ECHA. In , companies were required to disclose more information about nanomaterials. For example, various batteries on the European market contain nanomaterials, which will now need to be registered and evaluated by the ECHA.

This text has been produced for documentary purposes and the European Chemicals Agency does not assume any liability for its content. Please note that the text has no legal value. For legal purposes please refer to the texts published in the Official Journal of the European Union.

The consolidated version of the Test Methods regulation incorporates all the amendments and corrigenda set to the Regulation itself until the date marked in the first page of the document.

Consolidated version The consolidated version of the Fee Regulation incorporates all of the amendments and corrigenda to the Fee Regulation until the date marked in the first page of the regulation. The implementing legislation concerning the Board of Appeal and its functioning is available in the Appeals page. Further information related to the ongoing reviews and planned amendments to the REACH Annexes may be found on the websites of:.