摘要
目的探讨现行立法中假药定义存在的问题,为《药品管理法》的修订和完善提供参考。方法主要采用逻辑分析的方法,并结合各种类型药品的特点和药品标准的实际情况,通过分析得出结论。结果与结论现行《药品管理法》中的假药定义不能有效地适用于各种类型药品的假药判定,需要进行改进。
Objective To analyze the definition of counterfeit drugs in the Drug Administration Law of China, and provide references for the amendment and improvement of the Law. Methods By methods of logical analysis, with the consideration of the status of national standards and characteristics of different types of drugs. Results and Conclusions The definition of counterfeit drugs in the Drug Administration Law of China is not applicable to various types of drugs. The definition need to be amended.
出处
《中国药事》
CAS
2009年第8期745-747,共3页
Chinese Pharmaceutical Affairs
关键词
药品管理法
假药
定义
the Drug Administration Law of China
counterfeit drug
definition
