{
  "url": "https://openlegislation.uk/eu-regulation-2010-1235/article-4",
  "json_url": "https://openlegislation.uk/eu-regulation-2010-1235/article-4.json",
  "legislation": "eur/2010/1235",
  "legislation_title": "Regulation (EU) No 1235/2010 of the European Parliament and of the Council of 15 December 2010 amending, as regards pharmacovigilance of medicinal products for human use, Regulation (EC) No 726/2004 laying down Community procedures for the authorisation and supervision of medicinal products for human and veterinary use and establishing a European Medicines Agency, and Regulation (EC) No 1394/2007 on advanced therapy medicinal products (Text with EEA relevance)",
  "legislation_url": "https://openlegislation.uk/eu-regulation-2010-1235",
  "path": "article/4",
  "kind": "article",
  "number": "4",
  "heading": "Entry into force and application",
  "text": "This Regulation shall enter into force on the day following its publication in the Official Journal of the European Union.\nIt shall apply from 2 July 2012.",
  "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/2010/1235/article/4",
    "retrieved_at": "2026-11-01T14:50:25.100090+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."
}