{
  "url": "https://openlegislation.uk/eu-regulation-2017-1569/chapter-IV",
  "json_url": "https://openlegislation.uk/eu-regulation-2017-1569/chapter-IV.json",
  "legislation": "eur/2017/1569",
  "legislation_title": "Commission Delegated Regulation (EU) 2017/1569 of 23 May 2017 supplementing Regulation (EU) No 536/2014 of the European Parliament and of the Council by specifying principles of and guidelines for good manufacturing practice for investigational medicinal products for human use and arrangements for inspections (Text with EEA relevance)",
  "legislation_url": "https://openlegislation.uk/eu-regulation-2017-1569",
  "path": "chapter/IV",
  "kind": "chapter",
  "number": "IV",
  "heading": "FINAL PROVISIONS",
  "text": null,
  "extent": "E+W+S+N.I.",
  "status": null,
  "version": "current",
  "annotations": [],
  "outstanding_effects": [],
  "provenance": {
    "source": "legislation.gov.uk",
    "source_url": "https://www.legislation.gov.uk/eur/2017/1569/chapter/IV",
    "retrieved_at": "2026-11-01T14:44:34.669471+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."
}