当前位置: 首页? 政策法规? 国外法规? (EU) No 2015/1491:就维吉霉素,修订法?EU) No 37/2010附录(amending Regulation (EU) No 37/2010 as regards the substance ‘virginiamycin?

(EU) No 2015/1491:就维吉霉素,修订法?EU) No 37/2010附录(amending Regulation (EU) No 37/2010 as regards the substance ‘virginiamycin?

扫描二维 分享好友和朋友圈
放大字体缩小字体2015-09-28 09:16:09 来源9a href="http://eur-lex.europa.eu/legal-content/EN/TXT/?uri=uriserv:OJ.L_.2015.231.01.0007.01.ENG" target="_blank" rel="nofollow">EUROPE浏览次数9span id="hits">2882
核心提示:关于制定鸡肉中维吉霉素最大残留限量的申请已提交至欧洲药品评价局。兽用药品委员会建议针对鸡肌肉、皮肤和脂肪、肝脏和肾脏制定维吉霉素最大残留限量,,并建议将维吉霉素在鸡肉中的最大残留限量应用到其它家禽类,但此规定不适用于产蛋鸡。因此,(EU) No 37/2010附件表格中增加家禽类中维吉霉素的最大残留限量,在家禽类肌肉、皮肤和脂肪、肝脏、肾脏中的限量值分别为10 μg/kg?0 μg/kg?0 μg/kg?0 μg/kg、/div>
发布单位
EUROPEAN COMMISSION
EUROPEAN COMMISSION
发布文号 (EU) No 2015/1491
发布日期 2015-09-03 生效日期 2015-11-03
有效性状?/th> 废止日期 暂无
备注 2015??日,欧盟发布委员会条例,就维吉霉素,修订(EU) No 37/2010号法规 关于制定禽肉中维吉霉素最大残留限量的申请已提交至欧洲药品评价局(EMA)。EMA建议制定维吉霉素在鸡肌肉、皮肤和脂肪、肝脏和肾脏中的最大残留限量,并建议将其应用到其它家禽类,但不适用于产蛋鸡。因此,(EU) No 37/2010附件表格中增加家禽中维吉霉素的最大残留限量,在家禽类肌肉、皮肤和脂肪、肝脏、肾脏中的限量值分别为10 g/kg?0 g/kg?0 g/kg?0 g/kg、/td>
  COMMISSION IMPLEMENTING REGULATION (EU) 2015/1491
  of 3 September 2015
  amending Regulation (EU) No 37/2010 as regards the substance virginiamycin
  (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 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)
  Virginiamycin is not yet included in this table.
  (4)
  An application for the establishment of MRLs for virginiamycin in chicken 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 virginiamycin in chicken, applicable to muscle, skin and fat, liver and kidney, provided that the substance is not used for animals from which eggs are produced for human consumption.
  (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 MRL for virginiamycin from chicken to poultry 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 3 November 2015.
  This Regulation shall be binding in its entirety and directly applicable in all Member States.
  Done at Brussels, 3 September 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

Virginiamycin

Virginiamycin factor S1

Poultry

10 g/kg

30 g/kg

10 g/kg

60 g/kg

Muscle

Skin and fat

Liver

Kidney

Not for use in animals from which eggs are produced for human consumption

Anti-infectious agents/Antibiotics


地区9/font>欧盟
标签9/font>评价最大残留限?nbsp;限量家禽
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 0.172 second(s), 10 queries, Memory 4.44 M
    Baidu
    map