{
  "url": "https://openlegislation.uk/eu-regulation-2016-1832/annex-I",
  "json_url": "https://openlegislation.uk/eu-regulation-2016-1832/annex-I.json",
  "legislation": "eur/2016/1832",
  "legislation_title": "Commission Implementing Regulation (EU) 2016/1832 of 17 October 2016 amending the model certificates for imports into the Union of meat preparations, meat products and treated stomachs, bladders and intestines, as well as fresh meat of domestic solipeds set out in Decisions 2000/572/EC and 2007/777/EC and Regulation (EU) No 206/2010 as regards public health requirements for residues (Text with EEA relevance)",
  "legislation_url": "https://openlegislation.uk/eu-regulation-2016-1832",
  "path": "annex/I",
  "kind": "annex",
  "number": "I",
  "heading": null,
  "text": "In Annex II to Decision 2000/572/EC, in the model animal and public health certificate for meat preparations intended for consignment to the European Union from third countries, the following point II.1.10 is added to the public health attestation in Part II:\n‘(2) [II.1.10.\nif containing material from domestic solipeds, the fresh meat used in the preparation of the meat preparations:\neither (2) [was obtained from domestic solipeds which immediately prior to slaughter had been kept for at least six months or since birth, if slaughtered at an age of less than six months, or since importation as food producing equidae from a Member State of the European Union, if imported less than six months prior to slaughter, in a third country:\n(a) in which the administration to domestic solipeds:\n(i) of thyrostatic substances, stilbenes, stilbene derivatives, their salts and esters, oestradiol 17β and its ester-like derivatives is prohibited;\n(ii) of other substances having oestrogenic, androgenic or gestagenic action and of beta-agonists is only allowed for:\ntherapeutic treatment as defined in Article 1(2)(b) of Directive 96/22/EC, where applied in conformity with Article 4(2) of that Directive, or\nzootechnical treatment as defined in Article 1(2)(c) of Directive 96/22/EC, where applied in conformity with Article 5 of that Directive; and\n(b) which has had, at least during the six months prior to slaughter of the animals, a plan for the monitoring of the groups of residues and substances referred to in Annex I to Directive 96/23/EC which covers equidae born in and imported into the third country and was approved in accordance with the fourth subparagraph of Article 29(1) of Directive 96/23/EC;]]\nand/or (2) [was imported from a Member State of the European Union.]]’",
  "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/eur/2016/1832/annex/I",
    "retrieved_at": "2026-11-01T14:45:25.729284+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."
}