explosives control law

Comparison between US FDCA and Drug Administration Law of PRC;

美国FDCA与我国药品管理法

Suggestion on the Revising of Drug Administration Law;

关于修改《药品管理法》的思考

“Drug Administration Law of PRC” and Protection for Human Rights;

《药品管理法》与人权保护

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

Results:The Drug Administration Law of China needs to be improved in aspects of the definition of new drug,the standards to divide the counterfeit drug and the adulterated drug,and the confirmation of the responsibility for the drug damage compensation.

目的:探讨我国药品安全监管中存在的法律问题,为《药品管理法》的再修订提供参考。

Objective:To provide suggestions for China in revising"Pharmaceutical Affairs Law"Methods:Through consulting the FD&CA and the FDA Import Procedures,the study was done by reviewing literature and comparison study.

目的:为我国《药事管理法》修订提供建议。

Since the implementation of categorization management of medicine in China, the medicine consume structure in our country has changed.

随着我国药品分类管理制度的实施，我国药品消费结构发生了变化，药品市场被细分为处方药市场和非处方药市场。

The consummation《Pharmaceutical Administration Law》revises Strengthens the Medical institutions drugs supervision

完善《药品管理法》修订 加强医疗机构药品监管

Sample Interpretation of Definition of Adulterated Drugand Misbranded Drug in Drug Management Law

浅析我国《药品管理法》对假劣药的界定

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

Comparison of Legal Liability between US FDCA and Drug Administration Law of PRC;

美国《食品、药品与化妆品法案》与我国《药品管理法》法律责任比较

the present Measures are formulated in accordance with the Pharmaceutical Administration Law of the People's Republic of China,

根据《中华人民共和国药品管理法》、

Pharmaceutical Administration Law of the People's Republic of China

中华人民共和国药品管理法

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

The Idea of Legislation in“Drug Administration Law of People's Republic of China”

《中华人民共和国药品管理法》立法理念探析

Some Proposals for Legislating Expired Drugs Recycling in“Drug Administration Law”of PRC

对我国《药品管理法》关于过期药品回收立法的若干建议

Suggestions on Drug Administration Law of People's Republic of China Amendment: Establishment of the Relief System of Adverse Drug Reaction

从建立药品不良反应损害救济制度浅谈《药品管理法》的完善

Some Suggestions on the Law Responsibility in the Act of Drug Administration

关于《药品管理法》之法律责任的修改建议

Amend the Pharmaceutical Administration Law,strengthen the linkage mechanism of drug administrative organs and criminal justice agencies

修订药品管理法,强化药品执法行刑联动机制——中美药品行刑联动机制比较研究

These Measures are formulated in accordance with the Pharmaceutical Administration Law of the People's Republic of China (hereinafter referred to as Pharmaceutical Administration Law).

根据《中华人民共和国药品管理法》（以下称《药品管理法》）的规定，制定本办法。

The inferior medicines referred to in this article mean those inferior pharmaceutical products that fall into the category of inferior medicines in accordance with the regulations of the "Law of the PRC Governing the Management of Pharmaceutical Products".

本条所称劣药，是指依照《中华人民共和国药品管理法》的规定属于劣药的药品。

Comprehensive Classified Management of Hospital Drug Storeroom

医院药库药品综合分类管理方法研究

Decree No. 6 of the State Food and Drug Administration of the People's Republic of China, Promulgating the Measures for the Administration of Business Licenses of Drugs

国家食品药品监督管理局令第6号,发布《药品经营许可证管理办法》

Inventory Control of Hospital Drug Based on ABC Classified Management & Virtual Drug Unit;

基于ABC分类管理法和虚拟药品单元的医院药品库存管理

The Regulation on Medicine Information Service via Internet

互联网药品信息服务管理办法