(EU) 2015/2062：就‘sisapronil’’这一物质，修订法规(EU) No 37/2010(amending Regulation (EU) No 37/2010 as regards

　　of 17 November 2015

　　amending Regulation (EU) No 37/2010 as regards the substance ‘sisapronil’

　　(Text with EEA relevance)

　　THE EUROPEAN COMMISSION,

　　Havin g regard to the Treaty on the Functio ning of the European Unio n,

　　Havin g 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 (1), and in particular Article 14 in co njunction with Article 17 thereof,

　　Havin g regard to the opinion of the European Medicines Agency formulated by the Committee for Medicinal Products for Veterinary Use,

　　Wher eas:

　　(1)

　　Article 17 of Regulation (EC) No 470/2009 requires that the maximum residue limit (hereinafter ‘MRL’) for pharmacologically active substances intended for use in the Unio n in veterinary medicinal products for food-producing animals or in biocidal products used in animal husbandry is established in a Regulation.

　　(2)

　　Table 1 of the Annex to Commission Regulation (EU) No 37/2010 (2) sets out the pharmacologically active substances and their classification regarding MRLs in foodstuffs of animal origin.

　　(3)

　　Sisapro nil is not yet included in that table.

　　(4)

　　An application for the establishment of MRLs for sisapro nil in bovine species has been submitted to the European Medicines Agency (hereinafter ‘EMA’).

　　(5)

　　The EMA, ba sed on the opinion of the Committee for Medicinal Products for Veterinary Use, has recommended the establishment of an MRL for sisapro nil in bovine species, applicable to muscle, fat, liver and kidney, provided that the substance is not used for animals from which milk is produced for human consumption.

　　(6)

　　According to Article 5 of Regulation (EC) No 470/2009, the EMA is to co nsider 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.

　　(7)

　　The EMA has co nsidered that the extrapolation of the MRL for sisapro nil from bovine to caprine species is appropriate.

　　(8)

　　Regulation (EU) No 37/2010 should therefore be amended accordingly.

　　(9)

　　It is appropriate to grant the stakeholders co ncerned a reaso nable period of time to take measures that may be required to comply with the new MRL.

　　(10)

　　The measures provided for in this Regulation are in accordance with the opinion of the Standing Committee on Veterinary Medicinal Products,

　　HAS ADOPTED THIS REGULATION:

　　Article 1

　　The Annex to Regulation (EU) No 37/2010 is amended as set out in the Annex to this Regulation.

　　Article 2

　　This Regulation shall enter into force on the twentieth day following that of its publication in the Official Journal of the European Unio n.

　　It shall apply from 17 January 2016.

　　This Regulation shall be binding in its entirety and directly applicable in all Member States.

　　Done at Brussels, 17 November 2015.

　　For the Commission

　　The President

　　Jean-Claude JUNCKER

　　(1) OJ L 152, 16.6.2009, p. 11.

　　(2) 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).

　　ANNEX

　　In Table 1 of the Annex to Regulation (EU) No 37/2010, an entry for the following substance is inserted in alphabetical order: