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我国药品监督的完善 被引量:1

Discussion the Improvement in Supervising the Drug of Our Country
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摘要 我国药品监管相关法律法规均已出台,但仍有相当数量因药品质量不合格引发病人伤亡的恶性事件不断发生,这不得不引发我们对当前我国药品产销各环节守法、执法效果的怀疑和思考。由行政许可制度的利弊分析引入我国药品监管的现状介绍,在步步深入的分析过程中,寻找目前我国药品监管在立法、执法等方面存在的问题。再结合对国外相关体制和立法、执法实践的分析,进一步认清我国药品监管目前存在的漏洞。当然,更重要的是在对比中借鉴实用的经验,探索解决问题的途径。 Although the laws and regulations located to medicine supervision have already been put into effect in China,there are still many malignant cases caused by unqualified medicine occurring one after another,which makes it worth for us to doubt and analyze the effect of law-enforcing in the chain of drug production and sale at present in our country.After analyzing the advantage and the disadvantage in the system of administrative license,the article introduces the present situation hereof and tries to discove...
作者 王飞
出处 《河北理工大学学报(社会科学版)》 2007年第S1期29-32,共4页 Journal of Hebei Polytechnic University:Social Science Edition
关键词 行政许可 我国药品监管制度 外国药品监管制度 administrative license the system of drug administration in China the system of drug administration in foreign countries
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