{
  "url": "https://openlegislation.uk/eu-regulation-2014-536/annex-III/division-2/division-2.3/division-11",
  "json_url": "https://openlegislation.uk/eu-regulation-2014-536/annex-III/division-2/division-2.3/division-11.json",
  "legislation": "eur/2014/536",
  "legislation_title": "Regulation (EU) No 536/2014 of the European Parliament and of the Council of 16 April 2014 on clinical trials on medicinal products for human use, and repealing Directive 2001/20/EC (Text with EEA relevance)",
  "legislation_url": "https://openlegislation.uk/eu-regulation-2014-536",
  "path": "annex/III/division/2/division/2.3/division/11",
  "kind": "division",
  "number": "11",
  "heading": "In addition, in order to properly process the report electronically, the following administrative information shall be provided:",
  "text": "(a) the sender's (case) safety report unique identifier;\n(b) the receive date of the initial information from the primary source;\n(c) the receipt date of the most recent information;\n(d) the worldwide unique case identification number;\n(e) the sender identifier.",
  "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/2014/536/annex/III/division/2/division/2.3/division/11",
    "retrieved_at": "2026-11-01T14:47:39.363123+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."
}