摘要
本文结合药物制度研究与汉语言分析方法,从字义和产品内涵角度分析假药的定义,并结合我国现行法律制度对假药界定条款进行法条解析。本文研究认为"假"和"药"分别具有不同的内涵,目前从法律角度定义的假药概念是不完善的。建议应在现有假药定义基础上进行完善,同时结合字义内涵和立法目的对假药进行分类,并提出法条修改建议,为《药品管理法》的修订提供参考,以期合理完善假药定义,促进医药政策与产业健康发展。
The literal analysis was adopted to analyze the definition of counterfeit drugs,together with the connotation of product and the current provision of counterfeit drugs.We found that both ＂counterfeit＂ and ＂drug＂ had different meanings,and the definition of counterfeit drugs in law was imperfect.The paper suggested that the definition of counterfeit drugs should be modified,and counterfeit drug should be classified combining with the connotation and legislative purpose.In order to promote the development of pharmaceutical industry,this paper also provided some law amendments for improving‘ the pharmaceutical administration law’
出处
《中国卫生政策研究》
CSCD
2014年第8期37-41,共5页
Chinese Journal of Health Policy
关键词
假药
药品管理法
字义
产品内涵
Counterfeit drugs
Drug administration law
Literal meaning
Connotation of product
