{
  "legislation": {
    "id": "eur/2014/1252",
    "title": "Commission Delegated Regulation (EU) No 1252/2014 of 28 May 2014 supplementing Directive 2001/83/EC of the European Parliament and of the Council with regard to principles and guidelines of good manufacturing practice for active substances for medicinal products for human use (Text with EEA relevance) (revoked)",
    "short_title": "Regulation (EU) No 1252/2014 supplementing Directive 2001/83/EC of the European Parliament and of the Council…",
    "citation": "EU Regulation No 1252/2014",
    "type": "eur",
    "date": "2014-05-28",
    "revised": false,
    "unapplied_effects": 0,
    "url": "https://openlegislation.uk/eu-regulation-2014-1252",
    "json_url": "https://openlegislation.uk/eu-regulation-2014-1252.json"
  },
  "direction": "made_to",
  "changes": 1,
  "count": 1,
  "page": 1,
  "next": null,
  "results": [
    {
      "id": "uksi/2019/775",
      "title": "The Human Medicines (Amendment etc.) (EU Exit) Regulations 2019",
      "url": "https://openlegislation.uk/human-medicines-amendment-etc-eu-exit-regulations-2019",
      "changes": 1,
      "outstanding": 0,
      "changes_url": "https://openlegislation.uk/eu-regulation-2014-1252/changes.json?with=uksi%2F2019%2F775"
    }
  ],
  "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."
}