# Commission Regulation (EU) 2018/782 of 29 May 2018 establishing the methodological principles for the risk assessment and risk management recommendations referred to in Regulation (EC) No 470/2009 (Text with EEA relevance), Division III.3.11

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

Information from the metabolism study shall also allow comparison of the metabolites produced in the target animal species with those produced in the laboratory animals species in order to ensure that the major residues to which consumers will be exposed (i.e. the major metabolites produced in the target species) were adequately tested in the laboratory animal toxicity studies.

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Source: https://www.legislation.gov.uk/eur/2018/782/annex/I/division/III/division/III.3/division/III.3.11 (the official version)
Page: https://openlegislation.uk/eu-regulation-2018-782/annex-I/division-III/division-III.3/division-III.3.11
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.