# 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 55

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

The purpose of the evaluation is to establish whether or not the product complies with the criteria set down in point (b) of Article 19(1). The competent authority shall reach its conclusion as a result of the integration of the risks arising from each active substance together with the risks from each substance of concern present in the biocidal product, based on the assessment carried out in accordance with points 13 to 54 of this Annex.

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Source: https://www.legislation.gov.uk/eur/2012/528/annex/VI/division/4/division/1/division/55 (the official version)
Page: https://openlegislation.uk/eu-regulation-2012-528/annex-VI/division-4/division-1/division-55
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.