{
  "url": "https://openlegislation.uk/eu-decision-2016-1235/introduction",
  "json_url": "https://openlegislation.uk/eu-decision-2016-1235/introduction.json",
  "legislation": "eudn/2016/1235",
  "legislation_title": "Commission Implementing Decision (EU) 2016/1235 of 26 July 2016 authorising a laboratory in the Republic of Korea to carry out serological tests to monitor the effectiveness of rabies vaccines in dogs, cats and ferrets (notified under document C(2016) 4665) (Text with EEA relevance)",
  "legislation_url": "https://openlegislation.uk/eu-decision-2016-1235",
  "path": "introduction",
  "kind": "introduction",
  "number": null,
  "heading": "Introductory text",
  "text": "Commission Implementing Decision (EU) 2016/1235\nof 26 July 2016\nauthorising a laboratory in the Republic of Korea to carry out serological tests to monitor the effectiveness of rabies vaccines in dogs, cats and ferrets\n(notified under document C(2016) 4665)\n(Text with EEA relevance)\nTHE EUROPEAN COMMISSION,\nHaving regard to the Treaty on the Functioning of the European Union,\nHaving regard to Council Decision 2000/258/EC of 20 March 2000 designating a specific institute responsible for establishing the criteria necessary for standardising the serological tests to monitor the effectiveness of rabies vaccines, and in particular Article 3(2) thereof,\nWhereas:\n(1)\nDecision 2000/258/EC designates the Agence française de sécurité sanitaire des aliments (AFSSA) in Nancy, France, as the specific institute responsible for establishing the criteria necessary for standardising the serological tests to monitor the effectiveness of rabies vaccines. The AFSSA has now been integrated into the Agence nationale de sécurité sanitaire de l'alimentation, de l'environnement et du travail (ANSES) in France.\n(2)\nDecision 2000/258/EC provides, inter alia, that the ANSES is to appraise laboratories in third countries that have applied for approval to carry out serological tests to monitor the effectiveness of rabies vaccines.\n(3)\nThe authorisation granted on 9 February 2007 in accordance with Decision 2000/258/EC to Choong Ang Vaccine laboratory in Daejeon has been withdrawn in accordance with Commission Decision 2010/436/EU following the unfavourable appraisal report dated 29 September 2015 established by the ANSES for this laboratory and submitted to the Commission.\n(4)\nThe competent authority of the Republic of Korea has submitted an application for re-approval of Choong Ang Vaccine laboratory in Daejeon, and the ANSES has established and submitted to the Commission a favourable appraisal report dated 21 March 2016 for this laboratory.\n(5)\nThis laboratory should therefore be authorised to carry out serological tests to monitor the effectiveness of rabies vaccines in dogs, cats and ferrets.\n(6)\nThe measures provided for in this Decision are in accordance with the opinion of Standing Committee on Plants, Animals, Food and Feed,\nHAS ADOPTED THIS DECISION:",
  "extent": "E+W+S+N.I.",
  "status": null,
  "version": "current",
  "annotations": [
    {
      "type": "footnote",
      "label": "f1",
      "text": "OJ L 79, 30.3.2000, p. 40."
    },
    {
      "type": "footnote",
      "label": "f2",
      "text": "Commission Decision 2010/436/EU of 9 August 2010 implementing Council Decision 2000/258/EC as regards proficiency tests for the purposes of maintaining authorisations of laboratories to carry out serological tests to monitor the effectiveness of rabies vaccines (OJ L 209, 10.8.2010, p. 19)."
    }
  ],
  "outstanding_effects": [],
  "provenance": {
    "source": "legislation.gov.uk",
    "source_url": "https://www.legislation.gov.uk/eudn/2016/1235/introduction",
    "retrieved_at": "2026-11-01T15:13:53.404446+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."
}