{
  "url": "https://openlegislation.uk/human-medicines-regulations-2012/schedule-7/paragraph-8",
  "json_url": "https://openlegislation.uk/human-medicines-regulations-2012/schedule-7/paragraph-8.json",
  "legislation": "uksi/2012/1916",
  "legislation_title": "The Human Medicines Regulations 2012",
  "legislation_url": "https://openlegislation.uk/human-medicines-regulations-2012",
  "path": "schedule/7/paragraph/8",
  "kind": "paragraph",
  "number": "8",
  "heading": null,
  "text": "(1) The person must (subject to sub-paragraph (2)) have at least two years' practical experience in an undertaking authorised to manufacture medicinal products of—\n(a) qualitative analysis of medicinal products;\n(b) quantitative analysis of active substances; and\n(c) the testing and checking necessary to ensure the quality of medicinal products.\n(2) But—\n(a) if the person has completed a university course lasting at least five years, the minimum period of practical experience under this paragraph is one year; and\n(b) if the person has completed a university course lasting at least six years, the minimum period of practical experience under this paragraph is six months.",
  "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/7/paragraph/8",
    "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."
}