食品伙伴網(wǎng)訊   據(jù)歐盟網(wǎng)站消息，3月18日歐盟（發(fā)布（EU）No 2015/446號(hào)委員會(huì)條例，就硒酸鋇（barium  selenate）使用規(guī)格修訂（EU）No37/2010，本法規(guī)自發(fā)布之日起第20日生效。

    新條例規(guī)定，硒酸鋇無需制定MRL，但是不能用于注射。

    部分原文報(bào)道如下：

    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,

    原文鏈接：<http://eur-lex.europa.eu/legal-content/EN/TXT/?uri=uriserv%3AOJ.L_.2015.074.01.0018.01.ENG>