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  "id": "eudr/2001/82",
  "title": "Directive 2001/82/EC of the European Parliament and of the Council of 6 November 2001 on the Community code relating to veterinary medicinal products",
  "short_title": "Directive 2001/82/EC of the European Parliament and of the Council of 6 November 2001 on the Community code relating to veterinary medicinal products",
  "long_title": "Directive 2001/82/EC of the European Parliament and of the Council of 6 November 2001 on the Community code relating to veterinary medicinal products",
  "citation": "EU Directive 2001/82",
  "type": "eudr",
  "year": "2001",
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      "number": "PART 2:",
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      "path": "annex/I/title/I/part/2/division/A/division/3",
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      "path": "annex/I/title/I/part/2/division/A/division/3/division/3.1",
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      "heading": "In order to give ‘quantitative particulars’ of all the active substances of the veterinary medicinal products, it is necessary, depending on the pharmaceutical form concerned, to specify the mass, or the number of units of biological activity, either per dosage-unit or per unit of mass or volume, of each active substance.",
      "url": "https://openlegislation.uk/eu-directive-2001-82/annex-I/title-I/part-2/division-A/division-3/division-3.1",
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      "path": "annex/I/title/I/part/2/division/A/division/4",
      "kind": "division",
      "number": "4",
      "heading": "Development pharmaceutics",
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      "path": "annex/I/title/I/part/2/division/B",
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      "heading": "DESCRIPTION OF THE MANUFACTURING METHOD",
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      "path": "annex/I/title/I/part/2/division/C",
      "kind": "division",
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      "heading": "CONTROL OF STARTING MATERIALS",
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      "heading": "General requirements",
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      "path": "annex/I/title/I/part/2/division/C/division/1/division/1.1",
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      "heading": "Active substances listed in pharmacopoeias",
      "url": "https://openlegislation.uk/eu-directive-2001-82/annex-I/title-I/part-2/division-C/division-1/division-1.1/division-1.1.1",
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      "heading": "Active substances not in a pharmacopoeia",
      "url": "https://openlegislation.uk/eu-directive-2001-82/annex-I/title-I/part-2/division-C/division-1/division-1.1/division-1.1.2",
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      "path": "annex/I/title/I/part/2/division/C/division/1/division/1.1/division/1.1.3",
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      "heading": "Physico-chemical characteristics liable to affect bioavailability",
      "url": "https://openlegislation.uk/eu-directive-2001-82/annex-I/title-I/part-2/division-C/division-1/division-1.1/division-1.1.3",
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      "path": "annex/I/title/I/part/2/division/C/division/1/division/1.2",
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      "number": "1.2",
      "heading": "Excipients",
      "url": "https://openlegislation.uk/eu-directive-2001-82/annex-I/title-I/part-2/division-C/division-1/division-1.2",
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      "path": "annex/I/title/I/part/2/division/C/division/1/division/1.3",
      "kind": "division",
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      "heading": "Container-closure systems",
      "url": null,
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      "heading": "Finished product",
      "url": "https://openlegislation.uk/eu-directive-2001-82/annex-I/title-I/part-2/division-C/division-1/division-1.3/division-1.3.2",
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      "path": "annex/I/title/I/part/2/division/C/division/1/division/1.4",
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      "heading": "Substances of biological origin",
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      "number": "D",
      "heading": "CONTROL TESTS CARRIED OUT AT INTERMEDIATE STAGES OF THE MANUFACTURING PROCESS",
      "url": "https://openlegislation.uk/eu-directive-2001-82/annex-I/title-I/part-2/division-D",
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      "heading": "TESTS ON THE FINISHED PRODUCT",
      "url": "https://openlegislation.uk/eu-directive-2001-82/annex-I/title-I/part-2/division-E",
      "extent": "E+W+S+N.I.",
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      "path": "annex/I/title/I/part/2/division/E/division/1",
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      "number": "1",
      "heading": "General characteristics of the finished product",
      "url": "https://openlegislation.uk/eu-directive-2001-82/annex-I/title-I/part-2/division-E/division-1",
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      "path": "annex/I/title/I/part/2/division/E/division/2",
      "kind": "division",
      "number": "2",
      "heading": "Identification and assay of active substance(s)",
      "url": "https://openlegislation.uk/eu-directive-2001-82/annex-I/title-I/part-2/division-E/division-2",
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      "heading": "Identification and assay of excipient components",
      "url": "https://openlegislation.uk/eu-directive-2001-82/annex-I/title-I/part-2/division-E/division-3",
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      "path": "annex/I/title/I/part/2/division/E/division/4",
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      "heading": "Safety tests",
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      "path": "annex/I/title/I/part/2/division/F",
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      "heading": "STABILITY TEST",
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      "heading": "Active substances(s)",
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      "path": "annex/I/title/I/part/2/division/F/division/2",
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      "heading": "Finished product",
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      "path": "annex/I/title/I/part/2/division/G",
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      "heading": "OTHER INFORMATION",
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      "number": "CHAPTER I:",
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      "path": "annex/I/title/I/part/3/division/A/chapter/I/division/2",
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      "heading": "Pharmacology",
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      "heading": "Single-dose toxicity",
      "url": "https://openlegislation.uk/eu-directive-2001-82/annex-I/title-I/part-3/division-A/chapter-I/division-3/division-3.1",
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      "url": "https://openlegislation.uk/eu-directive-2001-82/annex-I/title-I/part-3/division-A/chapter-I/division-3/division-3.6",
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