摘要
目的:聚焦药品标准工作中存在的突出问题,从《药品管理法》法律层面提出改进建议。方法:对药品标准工作中存在的问题进行梳理,分析产生问题的原因,探讨在法律制度设计层面存在的不足,研究提出相关对策。结果:药品标准工作存在不同层级规定的衔接不畅、工作机制不够健全、职责部门权责不清等问题。结论:应以《药品管理法》修订为契机,在法律框架下统筹解决上述问题。
Objective:Focus on the questions existed in administration of drug standard, Put forward the improvement proposal from the legal level of the Drug Administration Law.Methods:The questions existed in administration of drug standard were analyzed, de-fects in legal system designing were paid more attentions, and then relevant suggestions were proposed.Results:Some questions exis-ted, such as the harmony of laws and regulations at different levels was unsatisfactory, drug standard′s working mechanism should be reformed, and the responsibilities of relevant departments should be made clear.Conclusion:The questions above should be resolved under the legal framework when revising the Drug Administration Law.
出处
《中国药品标准》
CAS
2016年第2期83-87,共5页
Drug Standards of China
关键词
药品标准
机制
药品管理法
修订
drug standard
working mechanism
Drug Administration Law
revise