{
  "url": "https://openlegislation.uk/medicines-act-1968-amendment-regulations-1992/regulation-2",
  "json_url": "https://openlegislation.uk/medicines-act-1968-amendment-regulations-1992/regulation-2.json",
  "legislation": "uksi/1992/604",
  "legislation_title": "The Medicines Act 1968 (Amendment) Regulations 1992",
  "legislation_url": "https://openlegislation.uk/medicines-act-1968-amendment-regulations-1992",
  "path": "regulation/2",
  "kind": "regulation",
  "number": "2",
  "heading": "Amendment of section 7 of the Act",
  "text": "(1) Section 7 of the Act (general provisions as to dealing with medicinal products) shall be amended as follows.\n(2) In subsection (5)(b) (under which a person responsible for the placing of certain kinds of medicinal product on the market in the United Kingdom is required to have a product licence) for “or ready-made veterinary drug” there shall be substituted “, a ready-made veterinary drug or an industrially produced medicinal product other than a veterinary drug”.\n(3) After subsection (6) there shall be inserted—\n“(6A) Where the product which a person is responsible for placing on the market in the United Kingdom is not a veterinary drug, subsection (5)(b) of this section shall not apply if the product is—\n(a) whole human blood, human blood plasma or blood cells of human origin,\n(b) a radiopharmaceutical in which the radionuclide is in the form of a sealed source, or\n(c) a homoeopathic medicinal product.\n(6B) Where the product which a person is responsible for placing on the market in the United Kingdom is a veterinary drug, subsection (5)(b) of this section shall not apply if the product is—\n(a) a vaccine, toxin or serum,\n(b) a product based on radioactive isotopes,\n(c) a product specially prepared for administration by a veterinary surgeon or veterinary practitioner to a particular animal or herd which is under his care,\n(d) a homoeopathic medicinal product, or\n(e) an additive for animal feeding stuffs to which the provisions of Council Directive 70/524/EEC apply.”.\n(4) In subsection (7) (definitions) for the words from the beginning to “(b)” there shall be substituted—\n“In this section—\n“proprietary medicinal product” means a ready-prepared medicinal product placed on the market in the United Kingdom under a special name and in a special pack;\n“radiopharmaceutical” means a medicinal product which, when ready for use, contains one or more radionuclides included for a medicinal purpose; and”.\n(5) In that subsection, in the definition of “ready-made veterinary drug”, the words from “and for the purposes of this definition” to the end are hereby repealed.",
  "extent": null,
  "status": null,
  "version": "current",
  "annotations": [
    {
      "type": "footnote",
      "label": "f1",
      "text": "Section 7 has been amended by S.I. 1977/1050 and S.I. 1983/1724."
    },
    {
      "type": "footnote",
      "label": "f2",
      "text": "OJ No. L270, 14.12.70, p. 1."
    }
  ],
  "outstanding_effects": [],
  "provenance": {
    "source": "legislation.gov.uk",
    "source_url": "https://www.legislation.gov.uk/uksi/1992/604/regulation/2",
    "retrieved_at": "2026-10-29T14:26:18.319014+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."
}