欧盟食品动物注射部位兽药残留指南概述  

Overview of European Guideline on Injection Site Residues of Food-producing Animals

作　　者：孙雷[1] 王亦琳[1] 叶妮[1] 张骊[1] 王鹤佳[1] SUN Lei;WANG Yi-lin;YE Ni;ZHANG Li;WANG He-jia(China Institute of Veterinary Drug Control,Beijing 100081,China)

机构地区：[1]中国兽医药品监察所,北京100081

出　　处：《中国兽药杂志》2023年第1期45-51,共7页Chinese Journal of Veterinary Drug

摘　　要：2022年3月25日,欧盟药品管理局(EMA)兽医药品委员会(CVMP)发布了食品动物注射部位兽药残留指南,并于2022年8月1日正式生效。该指南代替旧版的注射部位兽药残留指南(EMA/CVMP/542/03-FINAL)。本文就新发布指南的背景、适用范围、法律依据、评价方法、残留研究及相关定义等内容进行介绍。On 25 March, 2022, Guideline on injection site residues of food-producing animals was published by Committee for Veterinary Medicinal Products of European Medicines Agency, and came into effect on 1 August, 2022. This guideline replaced the former guideline on injection site residues(EMA/CVMP/542/03-FINAL). This paper outlines the background、scope、legal basis、assessment approach、residue studies and relevant definition of this guideline.

关 键 词：欧盟 注射部位 兽药残留 休药期 指南 

分 类 号：S851.66[农业科学—预防兽医学]