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欧盟委员会近日提出关于改进兽药产品以及加药饲料管理现状的立法提案。新提案涉及内容广泛:一此提案将废止并更新药用饲料生产、上市和使用中的过时指令,以便规范欧盟药用饲料的生产标准和销售,保证药用饲料只能使用授权兽药,且仅由指定药厂生产;二部分治疗人类感染的抗菌剂非授权不得对动物使用,以便应对动物耐药性问题和保证抗生素的有效性;三只有获得销售授权的药品才能进入市
The European Commission recently proposed a legislative proposal to improve the status of veterinary drug products and dosing of feedstuffs. The new proposal covers a wide range of topics: one proposal will repeal and update outdated directives on the production, marketing and use of medicated feeds in order to regulate the production standards and sales of medicinal feed in the European Union, to ensure that medicinal feeds can only be licensed veterinary drugs, and only Produced by the designated pharmaceutical companies; Part II Antibiotics for the treatment of human infections are not authorized for use by animals in order to deal with animal resistance issues and to ensure the effectiveness of antibiotics; Only three drugs with marketing authorization can enter the market