摘要
补充检验方法属于国家药品标准的一部分,在中药监管方面起到很重要的技术支撑作用。本文针对中药补充检验方法的法律地位、研究流程及其在市场监管中的作用进行了综述,概述了补充检验方法研究规定及相关要求,介绍了中药补充检验方法在中药掺伪造假、染色、增重、非法添加化学药品等方面的作用,并就存在的问题提出相关建议。
Supplementary testing methods,as part of the national drug standards,provide important technical support for the supervision of traditional Chinese medicine(TCM).This paper reviews the statutory requirements and study procedure for supplementary testing methods and their application in market supervision;summarizes regulations and related requirements about study of supplementary testing methods;introduces the application of supplementary testing methods in combating adulteration,dying,weight gain by inorganic salt,illegal addition of chemicals in TCM;and proposes relevant solutions.
作者
程显隆
李明华
郭晓晗
杨建波
荆文光
康荣
魏锋
马双成
CHENG Xian-long;LI Ming-hua;GUO Xiao-han;YANG Jian-bo;JING Wen-guang;KANG Rong;WEI Feng;MA Shuang-cheng(National Institutes for Food and Drug Control)
出处
《中国食品药品监管》
2022年第3期74-78,共5页
China Food & Drug Administration Magazine
关键词
药品标准
中药质量
掺伪造假
非法添加
补充检验方法
市场监管
drug standards
quality of TCM
adulteration
illegal addition of chemicals
supplementary testing methods
market supervision