{
  "url": "https://openlegislation.uk/human-medicines-regulations-2012/schedule-4/paragraph-11",
  "json_url": "https://openlegislation.uk/human-medicines-regulations-2012/schedule-4/paragraph-11.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/11",
  "kind": "paragraph",
  "number": "11",
  "heading": null,
  "text": "Where—\n(a) the manufacturer's licence relates to the assembly of a medicinal product;\n(b) the medicinal product is not manufactured by the licence holder; and\n(c) particulars of the name and address of the manufacturer of the product, or the person who imports the product, have been given by the licence holder to the licensing authority,\nthe licence holder must immediately notify the licensing authority in writing of any changes in the particulars.",
  "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/11",
    "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."
}