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(EU) 2015/1820:就‘二甘醇单乙醚’这一物质,修订法规(EU) No 37/2010附录(amending Regulation (EU) No 37/2010 as regards the substance ‘Diethylene glycol monoethyl ether’)

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放大字体  缩小字体 2015-10-15 03:49:20  来源:欧盟  浏览次数:3104
核心提示:2015年10月10日,欧盟发布委员会实施条例(EU) 2015/1820,对(EU) No 37/2010进行相应的修正,允许二甘醇单乙醚用于所有生产食品的动物物种。
发布单位
欧盟委员会
欧盟委员会
发布文号 (EU) 2015/1820
发布日期 2015-10-10 生效日期 暂无
有效性状态 废止日期 暂无
备注 20151010日,欧盟发布委员会条例,(EU)2015/1820,修订法规(EU) No 37/2010附录,其附录表1规定,允许对猪和反刍动物使用药理学活性物质二甘醇单乙醚。欧洲药品管理局收到一份关于修订现行二甘醇单乙醚条目的申请,兽药产品委员会(CVMP)建议扩大二甘醇单乙醚条目的使用范围到家禽中。根据(EC) No 470/20095条相关规定,欧洲药品管理局认为:二甘醇单乙醚用于所有生产食品的动物物种是适当的。因此,对(EU) No 37/2010附录表1二甘醇单乙醚条目进行相应的修订,将其“动物种类”中“所有反刍动物和猪”修订为“所有食品生产种类”。

   COMMISSION IMPLEMENTING REGULATION (EU) 2015/1820
 
  of 9 October 2015
 
  amending Regulation (EU) No 37/2010 as regards the substance ‘Diethylene glycol monoethyl ether’
 
  (Text with EEA relevance)
 
  THE EUROPEAN COMMISSION,
 
  Having regard to the Treaty on the Functioning of the European Union,
 
  Having 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 conjunction with Article 17 thereof,
 
  Having regard to the opinion of the European Medicines Agency formulated by the Committee for Medicinal Products for Veterinary Use,
 
  Whereas:
 
  (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 Union in veterinary medicinal products for food-producing animals or in biocidal products used in animal husbandry is to be 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)
 
  Diethylene glycol monoethyl ether is currently included in that table as an allowed substance, for all ruminants and porcine species. According to the existing entry for diethylene glycol monoethyl ether, no MRL is required for these animal species.
 
  (4)
 
  An application for the extension of the existing entry for diethylene glycol monoethyl ether to poultry has been submitted to the European Medicines Agency (hereinafter ‘EMA’).
 
  (5)
 
  The EMA, based on the opinion of the Committee for Medicinal Products for Veterinary Use, has recommended the extension of the existing entry for diethylene glycol monoethyl ether to poultry.
 
  (6)
 
  According 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.
 
  (7)
 
  The EMA has considered that the extrapolation of the existing entry for diethylene glycol monoethyl ether to all food producing species is appropriate.
 
  (8)
 
  Regulation (EU) No 37/2010 should therefore be amended accordingly.
 
  (9)
 
  It is appropriate to grant the stakeholders concerned a reasonable 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 Union.
 
  It shall apply from 9 December 2015.
 
  This Regulation shall be binding in its entirety and directly applicable in all Member States.
 
  Done at Brussels, 9 October 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, the entry for the substance ‘diethylene glycol monethyl ether’ is replaced by the following:

Pharmacologically active Substance

Marker residue

Animal Species

MRLs

Target Tissues

Other Provisions (according to Article 14(7) of Regulation (EC) No 470/2009)

Therapeutic Classification

‘Diethylene glycol monethyl ether

NOT APPLICABLE

All food producing species

No MRL required

NOT APPLICABLE

NO ENTRY

NO ENTRY’

 
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