{
  "url": "https://openlegislation.uk/eu-directive-2004-73/annex-n4/division-B.1/division-3/division-3.1",
  "json_url": "https://openlegislation.uk/eu-directive-2004-73/annex-n4/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/n4/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 the 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 the 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/n4/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."
}