{
  "url": "https://openlegislation.uk/eu-directive-2004-73/annex-2B/division-B.1/division-3/division-3.1",
  "json_url": "https://openlegislation.uk/eu-directive-2004-73/annex-2B/division-B.1/division-3/division-3.1.json",
  "legislation": "eudr/2004/73",
  "legislation_title": "Commission Directive 2004/73/EC of 29 April 2004 adapting to technical progress for the twenty-ninth time Council Directive 67/548/EEC on the approximation of the laws, regulations and administrative provisions relating to the classification, packaging and labelling of dangerous substances (Text with EEA relevance)",
  "legislation_url": "https://openlegislation.uk/eu-directive-2004-73",
  "path": "annex/2B/division/B.1/division/3/division/3.1",
  "kind": "division",
  "number": "3.1",
  "heading": "Test report",
  "text": "The test report must include the following information, as appropriate:\nTest substance:\nphysical nature, purity, and, where relevant, physico-chemical properties (including isomerisation);\nidentification data, including CAS number.\nVehicle (if appropriate):\njustification for choice of vehicle, if other than water.\nTest animals:\nspecies/strain used;\nmicrobiological status of the animals, when known;\nnumber, age and sex of animals (including, where appropriate, a rationale for use of males instead of females);\nsource, housing conditions, diet etc.;\nTest conditions:\ndetails of test substance formulation, including details of the physical form of the material administered;\ndetails of the administration of the test substance including dosing volumes and time of dosing;\ndetails of food and water quality (including diet type/source, water source);\nthe rationale for the selection of the starting dose.\nResults:\ntabulation of response data and dose level for each animal (i.e. animals showing signs of toxicity including mortality, nature, severity and duration of effects);\ntabulation of body weight and body weight changes;\nindividual weights of animals at the day of dosing, in weekly intervals thereafter, and at time of death or sacrifice;\ndate and time of death if prior to scheduled sacrifice.\ntime course of onset of signs of toxicity and whether these were reversible for each animal;\nnecropsy findings and histopathological findings for each animal; if available.\nDiscussion and interpretation of results.\nConclusions.",
  "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/2004/73/annex/2B/division/B.1/division/3/division/3.1",
    "retrieved_at": "2026-11-01T15:22:47.605967+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."
}