欧盟动物源性产品中药物残留限量沿革分析
Evolution Analysis of Drug Residues in Animal Derived Products in EU
程坚1
作者信息
- 1. 安徽省食品药品检验研究院,安徽合肥230051
- 折叠
摘要
欧盟经过多年的发展,制订了《食品卫生法》等多部食品安全领域的制度法规,这些制度法规是欧盟保障食品安全的法律基础.将我国与欧盟的动物源性产品中药物残留限量进行对比分析,结合我国国情及进出口大宗动物源性产品情况,学习并借鉴欧盟的药物残留限值设置方式方法,促进我国药物残留标准体系的健全完善.
Abstract
After years of development,EU establishes many laws and regulations in the field of food safety,such as Food Hygiene Law.These laws and regulations are legal basis for EU to ensure the safety of food.In this research,we compared the residue limits of Traditional Chinese Medicine in animal-source products between China and EU,so as to learn from the design method for drug residues in EU.According to the situation of main animal-source products and the current situation of China,drug residues standard system could be improved by referring to the design of limit value in EU.
关键词
欧盟/动物源性产品/药物残留限量/沿革分析Key words
EU/Animal-source products/Drug residue limits/Evolution analysis引用本文复制引用
出版年
2016
国家科技期刊平台
NSTL
维普
万方数据