当前位置: 首页? 政策法规? 国外法规? (EU) 2015/1079:就药理学活性物质六?hexaflumuro),修?EU) No 37/2010号法规(amending Regulation (EU) No 37/2010 as regards the substance ‘hexaflumuron’)

(EU) 2015/1079:就药理学活性物质六?hexaflumuro),修?EU) No 37/2010号法规(amending Regulation (EU) No 37/2010 as regards the substance ‘hexaflumuron’)

扫描二维 分享好友和朋友圈
放大字体缩小字体2015-07-06 09:45:44 来源9a href="http://eur-lex.europa.eu/legal-content/EN/TXT/?uri=uriserv:OJ.L_.2015.175.01.0008.01.ENG" target="_blank" rel="nofollow">欧盟浏览次数9span id="hits">2809
核心提示?015??日,,欧盟发布委员会实施条例(EU) 2015/1079,对(EU) No 37/2010进行修正。在附录?中增加六氟在鳍鱼中的最大残留限量规定,其限量值为500μg/kg、/div>
发布单位
欧盟委员
欧盟委员伙/div>
发布文号 (EU) 2015/1079
发布日期 2015-07-04 生效日期 2015-07-24
有效性状?/th> 废止日期 暂无
备注
2015??日,,欧盟发布委员会实施条例(EU) 2015/1079,对(EU) No 37/2010进行修正。在附录?中增加六氟在鳍鱼中的最大残留限量规定,其限量值为500g/kg、/div>
  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 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)
  Hexaflumuron is not yet included in this table.
  (4)
  An application for the establishment of MRLs for hexaflumuron in fin fish 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 establishment of a MRL for hexaflumuron for fin fish, applicable to muscle and skin in natural proportions.
  (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, 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.
  (8)
  Table 1 of the Annex to Regulation (EU) No 37/2010 should therefore be amended accordingly.
  (9)
  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 2 September 2015.
  This Regulation shall be binding in its entirety and directly applicable in all Member States.
  Done at Brussels, 3 July 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:

Pharmacologically active Substance

Marker residue

Animal Species

MRL

Target Tissues

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

Therapeutic Classification

Hexaflumuron

Hexaflumuron

Fin fish

500 g/kg

Muscle and skin in natural proportions

NO ENTRY

Antiparasitic agents/Agents (acting) against ectoparasites

地区9/font>欧盟
标签9/font>活性物?nbsp;最大残留限?nbsp;限量
食品伙伴网提供标准法规解读、舆情监控、合规咨询、申报注册等服务、br/>电询?535-2129301
QQ?891238009
食品标法? border=
实时把握 食品标法动?/span>
请扫码关?span class="color2">食品标法圇/span>

声明9/p>

凡本网所有原?编译文章及图片、图表的版权均属食品伙伴网所有,如要转载,需注明“信息来源:食品伙伴网”、br> 凡本网注明“信息来源:XXX(非食品伙伴网)”的作品,均转载自其他媒体,转载目的在于传递更多的信息,并不代表本网赞同其观点和对其真实性负责、br> 邮箱:law#www.sqrdapp.com(发邮件时请?换成@ QQ?39307733

[ 政策法规搜索] [ 加入收藏] [ 告诉好友] [ 打印本文] [ 关闭窗口]


按分类浏觇/strong>
推荐国外法规
点击排行
    按国家或地区浏览

    法规中心 关于我们 广告业务 联系我们 信息服务

    Processed in 0.176 second(s), 10 queries, Memory 4.47 M
    Baidu
    map