1.
The Developing History of Drug s GMP and the Working Programme of Practicing GMP;
药品GMP发展史及实施GMP的工作程序
2.
The analysis of the implementation of pharmaceutical GMP model on specie-specific patterns
浅析以品种为单元的药品GMP实施模式
3.
Research on Implement and Development of Good Manufacturing Practice of Drug in China in New Era;
新时期我国药品GMP实施与发展研究
4.
Contrast Research Report of Domestic and Foreign Drug GMP (2);
国内外药品GMP对比调研报告(二)
5.
Contrast Research Report of Domestic and Foreign Drug GMP (1);
国内外药品GMP对比调研报告(一)
6.
Study on the Economy-law Effects of the Good Manufacturing Practice(GMP) for Drugs in China;
对我国药品GMP认证的经济法思考
7.
Update of Concept is important to better implementation of GMP
深入实施药品GMP管理贵在观念更新
8.
Pay Close Attention to the Anew Authentication of Drugs GMP
重视和做好药品GMP重新认证工作
9.
The Brief Analysis of Risk and Legal Liability of Drug GMP Certification
药品GMP认证的风险及法律责任浅析
10.
Contrast Research Report of Domestic and Foreign Drug GMP(5～6)
国内外药品GMP对比调研报告(五～六)
11.
Contrast Research Report of Domestic and Foreign Drug GMP (4)
国内外药品GMP对比调研报告(四)
12.
The Problems Which Should be Especially Concerned in Drug GMP Authentic Examination;
药品GMP认证现场检查时应特别关注的问题
13.
Study the trend of materials management according to the revision of China's GMP of Drugs
从我国药品GMP的修订看物料管理的动向
14.
Application of quality risk management (QRM) in drug GMP site inspection
质量风险管理在药品GMP现场检查中运用的探讨
15.
Ideas and Prospects of Application of Remote Diagnosis and Distance Education in the Management of GMP;
远程诊断和远程教育在药品GMP管理中应用的设想与展望
16.
The Study of Pharmaceutical Enterprise Drawing Lessons from TQM to Consummate GMP;
药品生产企业借鉴TQM完善GMP研究
17.
Main Differences between GMP Requirements of EU and Non-bacteria Drug Production in China;
我国无菌药品生产与欧盟GMP要求的主要不同点
18.
Discussion on the Methods and Skills for Implementation of GMP Self Inspection in the Drug Production Enterprises;
浅谈药品生产企业实施GMP自检的方法和技巧