{
  "url": "https://openlegislation.uk/eu-directive-2008-73/annex",
  "json_url": "https://openlegislation.uk/eu-directive-2008-73/annex.json",
  "legislation": "eudr/2008/73",
  "legislation_title": "Council Directive 2008/73/EC of 15 July 2008 simplifying procedures of listing and publishing information in the veterinary and zootechnical fields and amending Directives 64/432/EEC, 77/504/EEC, 88/407/EEC, 88/661/EEC, 89/361/EEC, 89/556/EEC, 90/426/EEC, 90/427/EEC, 90/428/EEC, 90/429/EEC, 90/539/EEC, 91/68/EEC, 91/496/EEC, 92/35/EEC, 92/65/EEC, 92/66/EEC, 92/119/EEC, 94/28/EC, 2000/75/EC, Decision 2000/258/EC and Directives 2001/89/EC, 2002/60/EC and 2005/94/EC (Text with EEA relevance)",
  "legislation_url": "https://openlegislation.uk/eu-directive-2008-73",
  "path": "annex",
  "kind": "annex",
  "number": null,
  "heading": null,
  "text": "‘ANNEX I\nAFSSA, Nancy\nLaboratoire d’études sur la rage et la pathologie des animaux sauvages\nTechnopôle agricole et vétérinaire\nBP 40 009\n54220 Malzéville Cedex\nFrance\nANNEX II\nThe specific institute responsible for establishing the criteria necessary for standardising the serological test to monitor the action of rabies vaccines shall:\ncoordinate the establishment, improvement and standardisation of methods of serological titration on carnivores vaccinated against rabies,\nappraise those laboratories in Member States which have submitted an application to perform the serological titrations referred to in the first indent; the result of this appraisal must be sent to the applicant laboratory and to the competent authorities of the Member State where the result is favourable for the purposes of approval,\nappraise those laboratories in third countries which have submitted an application to perform the serological titrations referred to in the first indent; the result of this appraisal must be sent to the applicant laboratory and to the Commission where the result is favourable for the purpose of approval,\nprovide any useful information on analysis methods and comparative trials to those laboratories and organise training sessions and further training courses for their staff,\norganise inter-laboratory aptitude tests (proficiency tests),\nprovide scientific and technical assistance to the Commission and the competent authorities concerned on the matters referred to in this Annex, in particular in cases of disagreement on results of serological titrations.’",
  "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/eudr/2008/73/annex",
    "retrieved_at": "2026-11-01T15:22:19.455440+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."
}