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) (c. 528)

ANNEX III U.K. INFORMATION REQUIREMENTS FOR BIOCIDAL PRODUCTS

6. Tests performed should comply with the relevant requirements of protection of laboratory animals, set out in Directive 2010/63/EU and, in the case of ecotoxicological and toxicological tests, good laboratory practice, set out in Directive 2004/10/EC or other international standards recognised as being equivalent by the [F1 competent authority]. Tests on physico-chemical properties and safety-relevant substance data should be performed at least according to international standards. U.K.

Textual Amendments

F1 Words in Annex 3 para. 6 substituted (31.12.2020) by The Chemicals (Health and Safety) and Genetically Modified Organisms (Contained Use) (Amendment etc.) (EU Exit) Regulations 2019 (S.I. 2019/720), reg. 1(2), Sch. 2 para. 141(4); 2020 c. 1, Sch. 5 para. 1(1)