{
  "url": "https://openlegislation.uk/eu-regulation-2015-1079/introduction",
  "json_url": "https://openlegislation.uk/eu-regulation-2015-1079/introduction.json",
  "legislation": "eur/2015/1079",
  "legislation_title": "Commission Implementing Regulation (EU) 2015/1079 of 3 July 2015 amending Regulation (EU) No 37/2010 as regards the substance ‘hexaflumuron’ (Text with EEA relevance)",
  "legislation_url": "https://openlegislation.uk/eu-regulation-2015-1079",
  "path": "introduction",
  "kind": "introduction",
  "number": null,
  "heading": "Introductory text",
  "text": "Commission Implementing Regulation (EU) 2015/1079\nof 3 July 2015\namending Regulation (EU) No 37/2010 as regards the substance ‘hexaflumuron’\n(Text with EEA relevance)\nTHE EUROPEAN COMMISSION,\nHaving regard to the Treaty on the Functioning of the European Union,\nHaving regard to Regulation (EC) No 470/2009 of the European Parliament and of the Council of 6 May 2009 laying down Community procedures for the establishment of residue limits of pharmacologically active substances in foodstuffs of animal origin, repealing Council Regulation (EEC) No 2377/90 and amending Directive 2001/82/EC of the European Parliament and of the Council and Regulation (EC) No 726/2004 of the European Parliament and the Council, and in particular Article 14 in conjunction with Article 17 thereof,\nHaving regard to the opinion of the European Medicines Agency formulated by the Committee for Medicinal Products for Veterinary Use,\nWhereas:\n(1)\nArticle 17 of Regulation (EC) No 470/2009 requires that the maximum residue limit (hereinafter ‘MRL’) for pharmacologically active substances intended for use in the Union in veterinary medicinal products for food-producing animals or in biocidal products used in animal husbandry is established in a regulation.\n(2)\nTable 1 of the Annex to Commission Regulation (EU) No 37/2010 sets out the pharmacologically active substances and their classification regarding MRLs in foodstuffs of animal origin.\n(3)\nHexaflumuron is not yet included in this table.\n(4)\nAn application for the establishment of MRLs for hexaflumuron in fin fish has been submitted to the European Medicines Agency (hereinafter ‘EMA’).\n(5)\nThe EMA, based on the opinion of the Committee for Medicinal Products for Veterinary Use, has recommended the establishment of a MRL for hexaflumuron for fin fish, applicable to muscle and skin in natural proportions.\n(6)\nAccording to Article 5 of Regulation (EC) No 470/2009, the EMA is to consider using MRLs established for a pharmacologically active substance in a particular foodstuff for another foodstuff derived from the same species, or MRLs established for a pharmacologically active substance in one or more species for other species.\n(7)\nThe EMA has considered that, because of the more limited metabolism in fish compared to the metabolism in mammalian and avian species, the MRLs for hexaflumuron cannot be extrapolated from fin fish to other food producing species.\n(8)\nTable 1 of the Annex to Regulation (EU) No 37/2010 should therefore be amended accordingly.\n(9)\nThe measures provided for in this Regulation are in accordance with the opinion of the Standing Committee on Veterinary Medicinal Products,\nHAS ADOPTED THIS REGULATION:",
  "extent": "E+W+S+N.I.",
  "status": null,
  "version": "current",
  "annotations": [
    {
      "type": "footnote",
      "label": "f1",
      "text": "OJ L 152, 16.6.2009, p. 11."
    },
    {
      "type": "footnote",
      "label": "f2",
      "text": "Commission Regulation (EU) No 37/2010 of 22 December 2009 on pharmacologically active substances and their classification regarding maximum residue limits in foodstuffs of animal origin (OJ L 15, 20.1.2010, p. 1)."
    }
  ],
  "outstanding_effects": [],
  "provenance": {
    "source": "legislation.gov.uk",
    "source_url": "https://www.legislation.gov.uk/eur/2015/1079/introduction",
    "retrieved_at": "2026-11-01T14:46:36.432116+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."
}