drug administration law

discussion on the improvement of drug administration law from the simplified procedure of administrative penalty

从行政处罚简易程序浅谈药品管理法律的完善

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legal procedure for investigating and dealing with cases of violation of the drug administration law

查处违反《药品管理法》案件的执法程序浅谈

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combining with the actual status, some thoughts on studying the drug administration law of the people; s republic of china are given in the aspects of position, functions and legal responsibilities of institutes for drug control in drug supervision and management.

本文结合我国药品检验机构的现状，从药品检验机构的地位、职能、作用及法律责任等方面谈了学习《药品管理法》的体会。

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on features of new drug administration law

试论新《药品管理法》的特点

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results& conclusions: the registration and approval of drugs and their patents right protection were legally independent of each other, to which the drug administration law and patent law respectively are appli-cable.

结果与结论：药品注册审批与专利权保护是相对独立的法律关系，分别适用药品管理法和专利法；

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consideration of legislation of current drug administration law

对现行药品监督管理立法的思考

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according to drug administration law of the people's republic of china, drug inspecting result should be provided by the drug testing institution in the penalty notification for deteriorated and contaminated drugs.

根据《药品管理法》，变质或被污染药品按假药论处的处罚通知上必须载明药品质量检验结果。

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basic conditions in execution of ″ drug administration law ″

论《药品管理法》施行的基础条件

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analysis on definition of counterfeit drugs in the drug administration law of china

现行《药品管理法》中假药定义剖析

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the drug prices must be verified and established by the price administration department according to" price law", "drug administration law".

而药品价格由价格管理部门&国家发改委、物价局根据《价格法》、《药品管理法》进行审核和制定。

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implement the drug administration law in earnest and rectify the dispensing of pharmaceutical preparations

认真贯彻《药品管理法》努力搞好制剂整顿

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suggestion on modifying parts of items of drug administration law

对《药品管理法》部分条款进行修改的设想

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research progress on the defects and improvement of drug administration law

《药品管理法》缺陷与完善之研究进展

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according to the "drug administration law" provisions, drugs must be accompanied by instructions.

根据《药品管理法》明确规定，药品必须附有一份药品说明书。

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health administrative departments have the judicious powers according to the drug administration law.

《药品管理法》赋予了卫生行政部门行政司法裁决权。

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the label requirements, such as the required format, particulars and contents, are of great significance in the implementation of drug administration law, the investigation and seizure of adulterated drugs, and the assurance of safe and effective use of drugs in man.

提出了药品标签的统一的格式、栏目、内容的具体要求，对于全面实施《药品管理法》、查处假劣药品、保证人民用药安全有效有着重要意义。

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the achievement in the implementation of drug administration law for 13 years in guangdong province are summarized, the problems and their existing reasons are analyzed.

总结广东省贯彻执行《药品管理法》13年来取得的10个方面的主要成效，分析存在问题及原因。

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