# 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 1

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

This Annex sets out the information requirements that shall be included in the dossier for the biocidal product accompanying an application for the approval of an active substance in accordance with point (b) of Article 6(1) and the dossier accompanying an application for the authorisation of a biocidal product in accordance with point (a) of Article 20(1).

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Source: https://www.legislation.gov.uk/eur/2012/528/annex/III/division/n1 (the official version)
Page: https://openlegislation.uk/eu-regulation-2012-528/annex-III/division-n1
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.