{
  "url": "https://openlegislation.uk/human-medicines-amendment-regulations-2013/regulation-4",
  "json_url": "https://openlegislation.uk/human-medicines-amendment-regulations-2013/regulation-4.json",
  "legislation": "uksi/2013/1855",
  "legislation_title": "The Human Medicines (Amendment) Regulations 2013",
  "legislation_url": "https://openlegislation.uk/human-medicines-amendment-regulations-2013",
  "path": "regulation/4",
  "kind": "regulation",
  "number": "4",
  "heading": "Insertion of regulation A17",
  "text": "In Part 3, before the heading “Manufacturing and wholesale dealing” there is inserted—\n“Manufacture and distribution of medicinal products and active substances\nCHAPTER 1\nInterpretation\nInterpretation\nA17. In this Part “manufacture”, in relation to an active substance, includes any process carried out in the course of making the substance and the various processes of dividing up, packaging, and presentation of the active substance.\nCHAPTER 2”.",
  "extent": null,
  "status": null,
  "version": "current",
  "annotations": [],
  "outstanding_effects": [],
  "provenance": {
    "source": "legislation.gov.uk",
    "source_url": "https://www.legislation.gov.uk/uksi/2013/1855/regulation/4",
    "retrieved_at": "2026-10-29T00:46:46.454767+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."
}