{
  "url": "https://openlegislation.uk/eu-directive-2017-1572/article-14",
  "json_url": "https://openlegislation.uk/eu-directive-2017-1572/article-14.json",
  "legislation": "eudr/2017/1572",
  "legislation_title": "Commission Directive (EU) 2017/1572 of 15 September 2017 supplementing Directive 2001/83/EC of the European Parliament and of the Council as regards the principles and guidelines of good manufacturing practice for medicinal products for human use (Text with EEA relevance)",
  "legislation_url": "https://openlegislation.uk/eu-directive-2017-1572",
  "path": "article/14",
  "kind": "article",
  "number": "14",
  "heading": "Self-inspection",
  "text": "The manufacturer shall be required to conduct repeated self-inspections as part of the pharmaceutical quality system in order to monitor the implementation and respect of good manufacturing practice and to propose any necessary corrective measures and/or preventive actions. Records shall be maintained of such self-inspections and any corrective actions subsequently taken.",
  "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/eudr/2017/1572/article/14",
    "retrieved_at": "2026-11-01T15:21:32.042869+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."
}