{
  "url": "https://openlegislation.uk/veterinary-medicines-regulations-2007/schedule-6/paragraph-3",
  "json_url": "https://openlegislation.uk/veterinary-medicines-regulations-2007/schedule-6/paragraph-3.json",
  "legislation": "uksi/2007/2539",
  "legislation_title": "The Veterinary Medicines Regulations 2007",
  "legislation_url": "https://openlegislation.uk/veterinary-medicines-regulations-2007",
  "path": "schedule/6/paragraph/3",
  "kind": "paragraph",
  "number": "3",
  "heading": "Manufacture",
  "text": "(1) The product must have been manufactured by—\n(a) the holder of a manufacturing authorisation if manufactured in the United Kingdom;\n(b) the holder of a manufacturing authorisation issued under Directive 2001/82/EC if manufactured in another member State;\n(c) in the case of Australia, Canada, New Zealand, or Switzerland, the holder of an authorisation from the competent authority permitting him to manufacture medicinal products;\n(d) in the case of any other country, a manufacturer whose premises have been inspected and approved by an officer of the Secretary of State.\n(2) This paragraph does not apply until 1st November 2007.",
  "extent": null,
  "status": null,
  "version": "current",
  "annotations": [],
  "outstanding_effects": [],
  "provenance": {
    "source": "legislation.gov.uk",
    "source_url": "https://www.legislation.gov.uk/uksi/2007/2539/schedule/6/paragraph/3",
    "retrieved_at": "2026-10-29T03:44:29.692897+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."
}