{
  "url": "https://openlegislation.uk/eu-regulation-2005-111/article-13",
  "json_url": "https://openlegislation.uk/eu-regulation-2005-111/article-13.json",
  "legislation": "eur/2005/111",
  "legislation_title": "Council Regulation (EC) No 111/2005 of 22 December 2004 laying down rules for the monitoring of trade between the Union and third countries in drug precursors",
  "legislation_url": "https://openlegislation.uk/eu-regulation-2005-111",
  "path": "article/13",
  "kind": "article",
  "number": "13",
  "heading": null,
  "text": "1. The application for export authorisations referred to in Article 12 shall contain at least the following:\n(a) the names and addresses of the exporter, the importer in the third country or Northern Ireland, any other operator involved in the export operation or shipment, and the ultimate consignee;\n(b) the name of the scheduled substance as stated in the Annex or, in the case of a mixture or a natural product, its name and eight-digit CN code and the name of any scheduled substance, as stated in the Annex, contained in the mixture or in the natural product;\n(c) the quantity and weight of the scheduled substance and, in the case of a mixture or a natural product, the quantity, weight, and, if available, the percentage of any scheduled substance contained therein;\n(d) details of the transport arrangements, such as the expected date of dispatch, method of transport, name of the customs office where the customs declaration is to be made and, where available at this stage, identification of the means of transport, itinerary, expected point of exit from Great Britain and the point of entry into the importing country or Northern Ireland;\n(e) in the cases referred to in Article 17, a copy of the import authorisation issued by the country of destination or Northern Ireland; and\n(f) the number of the licence or registration referred to in Articles 6 and 7.\nAn application for an export authorisation for exports of scheduled substances listed in Category 4 of the Annex shall contain the information set out in points (a) to (e) of the first subparagraph.\n2. A decision on the application for an export authorisation shall be taken within a period of 15 working days from the date on which the competent authority considers the file to be complete.\nThat period shall be extended if, in the cases referred to in Article 17, the competent authorities are obliged to make further enquiries under the second subparagraph of that Article.",
  "extent": "E+W+S+N.I.",
  "status": null,
  "version": "current",
  "annotations": [
    {
      "type": "F",
      "label": "F1",
      "text": "Regulation revoked (N.I.) (29.6.2026) by The Controlled Drugs (Drug Precursors) (Amendment and Revocation) Regulations 2026 (S.I. 2026/607), reg. 1(1), Sch."
    },
    {
      "type": "F",
      "label": "F2",
      "text": "Words in Art. 13(1)(a) inserted (29.6.2026) by The Controlled Drugs (Drug Precursors) (Amendment and Revocation) Regulations 2026 (S.I. 2026/607), regs. 1(1), 6(11)(a)"
    },
    {
      "type": "F",
      "label": "F3",
      "text": "Words in Art. 13(1)(d) substituted (29.6.2026) by The Controlled Drugs (Drug Precursors) (Amendment and Revocation) Regulations 2026 (S.I. 2026/607), regs. 1(1), 6(11)(b)(i)"
    },
    {
      "type": "F",
      "label": "F4",
      "text": "Words in Art. 13(1)(d) inserted (29.6.2026) by The Controlled Drugs (Drug Precursors) (Amendment and Revocation) Regulations 2026 (S.I. 2026/607), regs. 1(1), 6(11)(b)(ii)"
    },
    {
      "type": "F",
      "label": "F5",
      "text": "Words in Art. 13(1)(e) inserted (29.6.2026) by The Controlled Drugs (Drug Precursors) (Amendment and Revocation) Regulations 2026 (S.I. 2026/607), regs. 1(1), 6(11)(c)"
    },
    {
      "type": "F",
      "label": "F6",
      "text": "Inserted by Regulation (EU) No 1259/2013 of the European Parliament and of the Council of 20 November 2013 amending Council Regulation (EC) No 111/2005 laying down rules for the monitoring of trade between the Community and third countries in drug precursors."
    }
  ],
  "outstanding_effects": [],
  "provenance": {
    "source": "legislation.gov.uk",
    "source_url": "https://www.legislation.gov.uk/eur/2005/111/article/13",
    "retrieved_at": "2026-11-01T14:54:54.786055+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."
}