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

关键词:  食品动物  药理活性物质  残留  分析方法  性能要求

Key words:  food-producing animals  pharmacologically active substances  residue  method of analysis  performance requirement

摘要:

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。

Abstract:

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.