# 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 1.1.2

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

Data on human health and environmental properties from experiments not carried out according to GLP or the relevant test methods.
Data shall be considered to be equivalent to data generated by the corresponding test methods if the following conditions are met:
(1) adequacy of the data for the purpose of classification and labelling and risk assessment;
(2) adequate and reliable coverage of the key parameters/endpoints foreseen to be investigated in the corresponding test methods;
(3) exposure duration comparable to or longer than the corresponding test methods if exposure duration is a relevant parameter;
(4) adequate and reliable documentation of the study is provided; and
(5) the study is performed using a system of quality assurance.

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Source: https://www.legislation.gov.uk/eur/2012/528/annex/IV/division/1/division/1.1/division/1.1.2 (the official version)
Page: https://openlegislation.uk/eu-regulation-2012-528/annex-IV/division-1/division-1.1/division-1.1.2
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.