{
  "url": "https://openlegislation.uk/eu-regulation-2017-1569/article-22",
  "json_url": "https://openlegislation.uk/eu-regulation-2017-1569/article-22.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": "article/22",
  "kind": "article",
  "number": "22",
  "heading": "Quality system",
  "text": "1. The competent authorities shall establish, implement and comply with a properly designed quality system for their inspectors. The quality system shall be updated as appropriate.\n2. Each inspector shall be informed of the standard operating procedures and of his duties, responsibilities and ongoing training requirements. Those procedures shall be kept up to date.",
  "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/article/22",
    "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."
}