{
  "url": "https://openlegislation.uk/eu-regulation-2017-556/article-3",
  "json_url": "https://openlegislation.uk/eu-regulation-2017-556/article-3.json",
  "legislation": "eur/2017/556",
  "legislation_title": "Commission Implementing Regulation (EU) 2017/556 of 24 March 2017 on the detailed arrangements for the good clinical practice inspection procedures pursuant to Regulation (EU) No 536/2014 of the European Parliament and of the Council (Text with EEA relevance)",
  "legislation_url": "https://openlegislation.uk/eu-regulation-2017-556",
  "path": "article/3",
  "kind": "article",
  "number": "3",
  "heading": "Quality system",
  "text": "1. Each Member State shall set up a properly designed quality system ensuring that the inspection procedures are observed and consistently monitored.\nMember States shall maintain those quality systems up to date.\n2. Each inspector shall have access to and comply with standard operating procedures, details of their duties, responsibilities and training requirements.",
  "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/2017/556/article/3",
    "retrieved_at": "2026-11-01T14:45:06.073231+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."
}