{
  "url": "https://openlegislation.uk/medical-devices-amendment-regulations-2008/regulation-9",
  "json_url": "https://openlegislation.uk/medical-devices-amendment-regulations-2008/regulation-9.json",
  "legislation": "uksi/2008/2936",
  "legislation_title": "The Medical Devices (Amendment) Regulations 2008",
  "legislation_url": "https://openlegislation.uk/medical-devices-amendment-regulations-2008",
  "path": "regulation/9",
  "kind": "regulation",
  "number": "9",
  "heading": "Amendment of regulation 16 of the principal Regulations",
  "text": "In regulation 16 of the principal Regulations (procedures for general medical devices for clinical investigations) —\n(a) in paragraph (1)(a)—\n“for “Sections 1 and 2” substitute “Sections 1 and 2.2”; and\n(b) after paragraph (10) add—\n“(11) The manufacturer, or their single authorised representative, shall—\n(a) notify the Secretary of State of the end of the clinical investigation; and\n(b) provide justification where premature termination has resulted.”.",
  "extent": null,
  "status": null,
  "version": "current",
  "annotations": [],
  "outstanding_effects": [],
  "provenance": {
    "source": "legislation.gov.uk",
    "source_url": "https://www.legislation.gov.uk/uksi/2008/2936/regulation/9",
    "retrieved_at": "2026-10-29T03:22:08.877648+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."
}