{
  "url": "https://openlegislation.uk/eu-directive-1981-852",
  "json_url": "https://openlegislation.uk/eu-directive-1981-852.json",
  "id": "eudr/1981/852",
  "title": "Council Directive 81/852/EEC of 28 September 1981 on the approximation of the laws of the Member States relating to analytical, pharmaco-toxicological and clinical standards and protocols in respect of the testing of veterinary medicinal products",
  "short_title": "Council Directive 81/852/EEC of 28 September 1981 on the approximation of the laws of the Member States relating to analytical, pharmaco-toxicological and clinical standards and protocols in respect of the testing of veterinary medicinal products",
  "long_title": null,
  "citation": "EU Directive 1981/852",
  "type": "eudr",
  "year": "1981",
  "number": "852",
  "version": "current",
  "date": "1981-09-28",
  "revised": false,
  "valid_from": null,
  "extent": null,
  "unapplied_effects": 7,
  "provisions": [],
  "outstanding_effects": [
    {
      "type": "completion",
      "affected_provisions": "Annex",
      "affecting": "eudr/1987/20",
      "affecting_title": "Council Directive 87/20/EEC of 22 December 1986 amending Directive 81/852/EEC on the approximation of the laws of the Member States relating to analytical, pharmaco- toxicological and clinical standards and protocols in respect of the testing of veterinary medicinal products",
      "affecting_provisions": "Directive"
    },
    {
      "type": "addition",
      "affected_provisions": "Art. 2 BI",
      "affecting": "eudr/1987/20",
      "affecting_title": "Council Directive 87/20/EEC of 22 December 1986 amending Directive 81/852/EEC on the approximation of the laws of the Member States relating to analytical, pharmaco- toxicological and clinical standards and protocols in respect of the testing of veterinary medicinal products",
      "affecting_provisions": "Directive"
    },
    {
      "type": "addition",
      "affected_provisions": "Art. 2 QUATER",
      "affecting": "eudr/1987/20",
      "affecting_title": "Council Directive 87/20/EEC of 22 December 1986 amending Directive 81/852/EEC on the approximation of the laws of the Member States relating to analytical, pharmaco- toxicological and clinical standards and protocols in respect of the testing of veterinary medicinal products",
      "affecting_provisions": "Directive"
    },
    {
      "type": "addition",
      "affected_provisions": "Art. 2 TER",
      "affecting": "eudr/1987/20",
      "affecting_title": "Council Directive 87/20/EEC of 22 December 1986 amending Directive 81/852/EEC on the approximation of the laws of the Member States relating to analytical, pharmaco- toxicological and clinical standards and protocols in respect of the testing of veterinary medicinal products",
      "affecting_provisions": "Directive"
    },
    {
      "type": "replacement",
      "affected_provisions": "Annex",
      "affecting": "eudr/1992/18",
      "affecting_title": "Commission Directive 92/18/EEC of 20 March 1992 modifying the Annex to Council Directive 81/852/EEC on the approximation of the laws of Member States relating to analytical, pharmacotoxicological and clinical standards and protocols in respect of the texting of veterinary medicinal products",
      "affecting_provisions": "Directive"
    },
    {
      "type": "amendment",
      "affected_provisions": "Art. 2 TER",
      "affecting": "eudr/1993/40",
      "affecting_title": "Council Directive 93/40/EEC of 14 June 1993 amending Directives 81/851/EEC and 81/852/EEC on the approximation of the laws of the Member States relating to veterinary medicinal products",
      "affecting_provisions": "Directive"
    },
    {
      "type": "completion",
      "affected_provisions": "Annex",
      "affecting": "eudr/1999/104",
      "affecting_title": "Commission Directive 1999/104/EC of 22 December 1999 amending the Annex to Council Directive 81/852/EEC on the approximation of the laws of the Member States relating to analytical, pharmacotoxicological and clinical standards and protocols in respect of the testing of veterinary medicinal products (Text with EEA relevance)",
      "affecting_provisions": "Directive"
    }
  ],
  "made_under": [],
  "changes_made_to": 7,
  "changes_made_to_url": "https://openlegislation.uk/eu-directive-1981-852/changes.json",
  "changes_made_by": 0,
  "changes_made_by_url": "https://openlegislation.uk/eu-directive-1981-852/changes/by-it.json",
  "instruments_made_under": 0,
  "instruments_made_under_url": "https://openlegislation.uk/eu-directive-1981-852/instruments.json",
  "provenance": {
    "source": "legislation.gov.uk",
    "source_url": "https://www.legislation.gov.uk/eudr/1981/852",
    "retrieved_at": "2026-11-01T15:23:39.035448+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."
}