{
  "url": "https://openlegislation.uk/eu-regulation-2019-6/annex-II/title-I/part-3/division-B/chapter-I/division-3",
  "json_url": "https://openlegislation.uk/eu-regulation-2019-6/annex-II/title-I/part-3/division-B/chapter-I/division-3.json",
  "legislation": "eur/2019/6",
  "legislation_title": "Regulation (EU) 2019/6 of the European Parliament and of the Council of 11 December 2018 on veterinary medicinal products and repealing Directive 2001/82/EC (Text with EEA relevance)",
  "legislation_url": "https://openlegislation.uk/eu-regulation-2019-6",
  "path": "annex/II/title/I/part/3/division/B/chapter/I/division/3",
  "kind": "division",
  "number": "3",
  "heading": "Residue analytical method",
  "text": "The analytical method(s) used in the residues depletion study (studies) and its (their) validation shall be described in detail.\nThe following characteristics shall be described:\nspecificity,\naccuracy,\nprecision,\nlimit of detection,\nlimit of quantification,\npracticability and applicability under normal laboratory conditions,\nsusceptibility to interference,\nstability of incurred residues.\nThe suitability of the analytical method proposed shall be evaluated in the light of the state of scientific and technical knowledge at the time the application is submitted.\nThe analytical method shall be presented in an internationally agreed format.",
  "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/2019/6/annex/II/title/I/part/3/division/B/chapter/I/division/3",
    "retrieved_at": "2026-11-01T14:43:40.425754+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."
}