{
  "url": "https://openlegislation.uk/eu-directive-2006-17/annex-II/division-2/division-2.6",
  "json_url": "https://openlegislation.uk/eu-directive-2006-17/annex-II/division-2/division-2.6.json",
  "legislation": "eudr/2006/17",
  "legislation_title": "Commission Directive 2006/17/EC of 8 February 2006 implementing Directive 2004/23/EC of the European Parliament and of the Council as regards certain technical requirements for the donation, procurement and testing of human tissues and cells (Text with EEA relevance)",
  "legislation_url": "https://openlegislation.uk/eu-directive-2006-17",
  "path": "annex/II/division/2/division/2.6",
  "kind": "division",
  "number": "2.6",
  "heading": null,
  "text": "If in a living donor (except bone marrow stem-cell and peripheral blood stem-cell donors) the ‘donation sample’, as defined in point 2(5)(a) above, is additionally tested by the nucleic acid amplification technique (NAT) for HIV, HBV and HCV, testing of a repeat blood sample is not required. Retesting is also not required if the processing includes an inactivation step that has been validated for the viruses concerned.",
  "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/2006/17/annex/II/division/2/division/2.6",
    "retrieved_at": "2026-11-01T15:22:38.416524+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."
}