# Regulation (EU) No 528/2012 of the European Parliament and of the Council of 22 May 2012 concerning the making available on the market and use of biocidal products (Text with EEA relevance), Division 13

Extent: E+W+S+N.I.

The data submitted in support of an application for authorisation of a biocidal product shall be validated by the ... competent authority in accordance with the relevant articles of the Regulation. After validation of these data the competent authority shall utilise them by carrying out a risk assessment based on the proposed use. Information submitted in the framework of Regulation (EC) No 1907/2006 shall be taken into account where appropriate.

---
Source: https://www.legislation.gov.uk/eur/2012/528/annex/VI/division/3/division/1/division/13 (the official version)
Page: https://openlegislation.uk/eu-regulation-2012-528/annex-VI/division-3/division-1/division-13
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.