{
  "url": "https://openlegislation.uk/human-medicines-amendment-supply-to-northern-ireland-regulations-2021/regulation-9",
  "json_url": "https://openlegislation.uk/human-medicines-amendment-supply-to-northern-ireland-regulations-2021/regulation-9.json",
  "legislation": "uksi/2021/1452",
  "legislation_title": "The Human Medicines (Amendment) (Supply to Northern Ireland) Regulations 2021",
  "legislation_url": "https://openlegislation.uk/human-medicines-amendment-supply-to-northern-ireland-regulations-2021",
  "path": "regulation/9",
  "kind": "regulation",
  "number": "9",
  "heading": "Amendment to regulation 39 (further requirements for manufacturer’s licence)",
  "text": "In regulation 39, substitute paragraph (8) with—\n“(8) In distributing a medicinal product by way of wholesale dealing, the licence holder must comply with the following as if they are a holder of a wholesale dealer’s licence—\n(a) regulations 43(1), (2) and (5), 43ZA and 44(5) and (6), and\n(b) regulation 43A, if applicable, where the product is being distributed in NI.”.",
  "extent": null,
  "status": null,
  "version": "current",
  "annotations": [
    {
      "type": "footnote",
      "label": "f1",
      "text": "Regulation 39, amended by S.I 2019/775; there are other amending instruments but none is relevant."
    }
  ],
  "outstanding_effects": [],
  "provenance": {
    "source": "legislation.gov.uk",
    "source_url": "https://www.legislation.gov.uk/uksi/2021/1452/regulation/9",
    "retrieved_at": "2026-10-28T22:05:31.553190+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."
}