当前位置: 首页? 政策法规? 国外法规? (EU) 2015/150:就药理学活性物质加米霉?gamithromycin),修?EU) No 37/2010附录(amending the Annex to Regulation (EU) No 37/2010 as regards the substance ‘gamithromycin?

(EU) 2015/150:就药理学活性物质加米霉?gamithromycin),修?EU) No 37/2010附录(amending the Annex to Regulation (EU) No 37/2010 as regards the substance ‘gamithromycin?

扫描二维 分享好友和朋友圈
放大字体缩小字体2015-02-10 11:41:01 来源9a href="http://eur-lex.europa.eu/legal-content/EN/TXT/?uri=uriserv:OJ.L_.2015.026.01.0010.01.ENG" target="_blank" rel="nofollow">EUROPE浏览次数9span id="hits">2860
核心提示?015??1日,欧盟发布委员会实施条?EU) 2015/150,修?EU) No 37/2010。在附录?中增加加米霉素在猪的肌肉、皮肤和脂肪(自然比例)、肝脏和肾脏中的最大残留限量规定,其限量值分别为100ug/kg?00ug/kg?00ug/kg?00ug/kg、/div>
发布单位
EUROPEAN COMMISSION
EUROPEAN COMMISSION
发布文号 (EU) 2015/150
发布日期 2015-01-31 生效日期 暂无
有效性状?/th> 废止日期 暂无
备注 2015??1日,欧盟发布委员会实施条?EU) 2015/150,修?EU) No 37/2010。在附录?中增加加米霉素在猪的肌肉、皮肤和脂肪(自然比例)、肝脏和肾脏中的最大残留限量规定,其限量值分别为100ug/kg?00ug/kg?00ug/kg?00ug/kg、/td>

  COMMISSION IMPLEMENTING REGULATION (EU) 2015/150

  of 30 January 2015

  amending the Annex to Regulation (EU) No 37/2010 as regards the substance gamithromycin

  (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 of 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)

  The maximum residue limit (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 accordance with Regulation (EC) No 470/2009.

  (2)

  Pharmacologically active substances and their classification regarding MRLs in foodstuffs of animal origin are set out in the Annex to Commission Regulation (EU) No 37/2010 (2).

  (3)

  Gamithromycin is currently included in Table 1 of the Annex to Regulation (EU) No 37/2010 as an allowed substance for bovine species, applicable to fat, liver and kidney, excluding animals producing milk for human consumption.

  (4)

  An application for the extension of the existing entry for gamithromycin to porcine species has been submitted to the European Medicines Agency.

  (5)

  In accordance with Article 5 of Regulation (EC) No 470/2009 the European Medicines Agency 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. The Committee for Medicinal Products for Veterinary Use concluded that the extrapolation to other food producing species cannot be supported for this substance.

  (6)

  The entry for gamithromycin in Table 1 of the Annex to Regulation (EU) No 37/2010 should therefore be amended to include the MRL for porcine species.

  (7)

  It is appropriate to provide for a reasonable period of time for the stakeholders concerned to take measures that may be required to comply with the newly set MRL.

  (8)

  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 1 April 2015.

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

  Done at Brussels, 30 January 2015.

  For the Commission

  The President

  Jean-Claude JUNCKER

ANNEX
In Table 1 of the Annex to Regulation (EU) No 37/2010, the entry for the substance gamithromycin 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
Gamithromycin
Gamithromycin
Porcine
100 g/kg
Muscle
NO ENTRY
Anti-infectious agents/Antibiotics
100 g/kg
Skin and fat in natural proportions
100 g/kg
Liver
300 g/kg
Kidney
Bovine
20 g/kg
Fat
Not for use in animals producing milk for human consumption.
200 g/kg
Liver
100 g/kg
Kidney


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 0.172 second(s), 10 queries, Memory 4.47 M
    Baidu
    map