# 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 7

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

Where testing is done, a detailed quantitative and qualitative description (specification) of the product used for each test and its impurities must be provided.

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Source: https://www.legislation.gov.uk/eur/2012/528/annex/III/division/7 (the official version)
Page: https://openlegislation.uk/eu-regulation-2012-528/annex-III/division-7
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.