{
  "url": "https://openlegislation.uk/human-medicines-regulations-2012/schedule-9/paragraph-7",
  "json_url": "https://openlegislation.uk/human-medicines-regulations-2012/schedule-9/paragraph-7.json",
  "legislation": "uksi/2012/1916",
  "legislation_title": "The Human Medicines Regulations 2012",
  "legislation_url": "https://openlegislation.uk/human-medicines-regulations-2012",
  "path": "schedule/9/paragraph/7",
  "kind": "paragraph",
  "number": "7",
  "heading": null,
  "text": "The manufacturer must make such adequate and suitable arrangements as are necessary for carrying out in accordance with the UK marketing authorisation any tests of the strength, quality or purity of the medicinal products to which the UK marketing authorisation relates.",
  "extent": null,
  "status": null,
  "version": "current",
  "annotations": [
    {
      "type": "F",
      "label": "F1",
      "text": "Word in Sch. 9 inserted (31.12.2020) by The Human Medicines (Amendment etc.) (EU Exit) Regulations 2019 (S.I. 2019/775), regs. 1, 52(3); 2020 c. 1, Sch. 5 para. 1(1)"
    }
  ],
  "outstanding_effects": [],
  "provenance": {
    "source": "legislation.gov.uk",
    "source_url": "https://www.legislation.gov.uk/uksi/2012/1916/schedule/9/paragraph/7",
    "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."
}