# 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.3.4

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

Guidance provided in VICH GL46: Studies to evaluate the metabolism and residue kinetics of veterinary drugs in food-producing animals: metabolism study to determine the quantity and identify the nature of residues shall be followed in order to monitor (quantify) the depletion of total residues and key metabolites over time. These studies shall normally be performed using radiolabelled drug.

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Source: https://www.legislation.gov.uk/eur/2018/782/annex/I/division/III/division/III.3/division/III.3.4 (the official version)
Page: https://openlegislation.uk/eu-regulation-2018-782/annex-I/division-III/division-III.3/division-III.3.4
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.