{
  "url": "https://openlegislation.uk/human-medicines-amendment-no-2-regulations-2014/regulation-3",
  "json_url": "https://openlegislation.uk/human-medicines-amendment-no-2-regulations-2014/regulation-3.json",
  "legislation": "uksi/2014/1878",
  "legislation_title": "The Human Medicines (Amendment) (No. 2) Regulations 2014",
  "legislation_url": "https://openlegislation.uk/human-medicines-amendment-no-2-regulations-2014",
  "path": "regulation/3",
  "kind": "regulation",
  "number": "3",
  "heading": "Amendment of regulation 48",
  "text": "In regulation 48(2) (definitions in relation to the Part on marketing authorisations), after the definition of “generic medicinal product” insert—\n““parallel import licence” means a licence that—\n(a) is granted by the licensing authority in compliance with the rules of European Union Law relating to parallel imports; and\n(b) authorises the holder to place on the market a medicinal product imported into the United Kingdom from another EEA State;”.",
  "extent": null,
  "status": null,
  "version": "current",
  "annotations": [],
  "outstanding_effects": [],
  "provenance": {
    "source": "legislation.gov.uk",
    "source_url": "https://www.legislation.gov.uk/uksi/2014/1878/regulation/3",
    "retrieved_at": "2026-10-29T00:09:33.447150+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."
}