{
  "url": "https://openlegislation.uk/human-medicines-regulations-2012/schedule-34/paragraph-12",
  "json_url": "https://openlegislation.uk/human-medicines-regulations-2012/schedule-34/paragraph-12.json",
  "legislation": "uksi/2012/1916",
  "legislation_title": "The Human Medicines Regulations 2012",
  "legislation_url": "https://openlegislation.uk/human-medicines-regulations-2012",
  "path": "schedule/34/paragraph/12",
  "kind": "paragraph",
  "number": "12",
  "heading": null,
  "text": "In section 87 (requirements as to containers)—\n(a) in subsection (1) for “section 85(2) of this Act” substitute “ subsection (3) ”; and\n(b) after subsection (2) insert—\n“(3) The purposes mentioned in subsection (1) are—\n(a) securing that medicinal products are correctly described and readily identifiable;\n(b) securing that any appropriate warning or other appropriate instruction or information is given, and that false or misleading information is not given, with respect to medicinal products;\n(c) promoting safety in relation to medicinal products.”",
  "extent": null,
  "status": null,
  "version": "current",
  "annotations": [
    {
      "type": "M",
      "label": "M1",
      "text": "Section 87(1) was amended by paragraph 44 of Part 1 of Schedule 8 to S.I. 2006/2407."
    }
  ],
  "outstanding_effects": [],
  "provenance": {
    "source": "legislation.gov.uk",
    "source_url": "https://www.legislation.gov.uk/uksi/2012/1916/schedule/34/paragraph/12",
    "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."
}