{
  "url": "https://openlegislation.uk/human-medicines-regulations-2012/schedule-4/paragraph-5",
  "json_url": "https://openlegislation.uk/human-medicines-regulations-2012/schedule-4/paragraph-5.json",
  "legislation": "uksi/2012/1916",
  "legislation_title": "The Human Medicines Regulations 2012",
  "legislation_url": "https://openlegislation.uk/human-medicines-regulations-2012",
  "path": "schedule/4/paragraph/5",
  "kind": "paragraph",
  "number": "5",
  "heading": null,
  "text": "The licence holder must inform the licensing authority of any change that the licence holder proposes to make to a person named in the licence as—\n(a) the person whose duty it is to supervise the manufacturing or assembling operations;\n(b) in charge of the animals from which are derived substances used in the production of the medicinal products being manufactured or assembled; or\n(c) responsible for the culture of living tissues used in the manufacture of the medicinal products being manufactured or assembled.",
  "extent": null,
  "status": null,
  "version": "current",
  "annotations": [],
  "outstanding_effects": [],
  "provenance": {
    "source": "legislation.gov.uk",
    "source_url": "https://www.legislation.gov.uk/uksi/2012/1916/schedule/4/paragraph/5",
    "retrieved_at": "2026-10-29T01:24:34.993203+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."
}