{
  "url": "https://openlegislation.uk/eu-regulation-2018-782/annex-I/division-III/division-III.3/division-III.3.8",
  "json_url": "https://openlegislation.uk/eu-regulation-2018-782/annex-I/division-III/division-III.3/division-III.3.8.json",
  "legislation": "eur/2018/782",
  "legislation_title": "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)",
  "legislation_url": "https://openlegislation.uk/eu-regulation-2018-782",
  "path": "annex/I/division/III/division/III.3/division/III.3.8",
  "kind": "division",
  "number": "III.3.8",
  "heading": null,
  "text": "A suitable marker residue shall be identified. The marker residue may be the parent drug, any of its metabolites or a combination of any of these. The marker residue shall have the following properties:\n(a)it shall have a known relationship between it and the total residue concentration in the edible tissue/food commodity of interest;\n(b)it is appropriate for use in testing for the presence of residues at the time point of interest;\n(c)it shall have a practicable analytical method to measure it at the level of the MRL.",
  "extent": "E+W+S+N.I.",
  "status": null,
  "version": "current",
  "annotations": [],
  "outstanding_effects": [],
  "provenance": {
    "source": "legislation.gov.uk",
    "source_url": "https://www.legislation.gov.uk/eur/2018/782/annex/I/division/III/division/III.3/division/III.3.8",
    "retrieved_at": "2026-11-01T14:44:06.594245+00:00"
  },
  "licence": "Open Government Licence v3.0",
  "licence_url": "https://www.nationalarchives.gov.uk/doc/open-government-licence/version/3/",
  "attribution": "Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives."
}