欧盟关于食品动物用药理活性物质残留分析执行条例(EU)2021/808概述

Overview of Commission Implementing Regulation(EU)2021/808 on the Analysis for Residues of Pharmacologically Active Substances Used in Food-producing Animals

2021年3月22日,欧盟官方公报发布了欧盟委员会执行条例(EU)2021/808《食品动物用药理活性物质残留分析方法的性能、结果解释和采样方法》。该条例替代欧盟法规2002/657/EC和98/179/EC,自欧盟官方公报发布后第20日即从2021年5月21日起生效。本文概述了新法规(EU)2021/808的主要内容,重点介绍了食品动物用药理活性物质残留分析方法的性能要求。该法规的发布实施,对我国从事动物性食品等产品中药物残留分析有很强的借鉴意义。

On 22 March,2021,Official Journal of the European Union published commission implementing regulation(EU)2021/808,“on the performance of analytical methods for residues of pharmacologically active substances used in food-producing animals and on the interpretation of results as well as on the methods to be used for sampling and repealing Decisions 2002/657/EC and 98/179/EC”.The regulation replaced decisions 2002/657/EC and 98/179/EC and should enter into force on the twentieth day following that of its publication in the Official Journal of the European Union.This paper outlines the main contents of new regulation(EU)2021/808 and focuses on the performance of analytical methods for residues of pharmacologically active substances used in food-producing animals.The promulgation and implementation of the regulation have a strong reference significance for our country to engage in the analysis of drug residues in animal derived food.