1.
Guarantee Role of Information Technology in the Drug Technological Evaluation Process
信息技术对我国药品技术审评工作的保障作用
2.
The Necessity of GLP Implementation From Point View of Drug Technical Evaluation;
从药品技术审评的角度看GLP实施的必要性
3.
A Study on the Hi-tech Product Development Based on Graphical Evaluation and Review Technology;
基于图示评审技术GERT的高科技产品开发研究
4.
Modeling of product development process with graphical evaluation and review technique;
产品开发过程的图示评审技术建模方法
5.
The insights on post-marketing evaluation in China;
关于我国药品上市后评价技术工作的思考
6.
PERT (Program Evaluation and Review Technic)
计划评价与审查技术
7.
Technique obstacles of using Pharmacoeconomics evaluation to help the drug price making;
在我国药品定价中应用药物经济学评价的技术性障碍分析
8.
National Committee on the assessment of protected traditional Chinese medicinal products
国家中药品种保护审评委员会
9.
Study on Determination and Safety Assessment of Perfluorooctane Sulfonate (PFOS) in Drug Packaging Materials
药品包装材料中全氟辛烷磺酸类物质检测与安全评价技术
10.
On the Construction of China s Medicine Evaluation Advisory Committee Systems;
论我国药品审评咨询委员会制度的构建
11.
Discussion on the Revelatory Effects of Canada s CDR System to China;
加拿大的共同药品审评(CDR)制度及对我国的启示
12.
GSP Interior Appraisal of Request,Procedure and Key in the Drugs Management Enterprise
药品经营企业GSP内部评审的要求、程序及重点
13.
Problem analysis of residual solvents control in drug evaluation
药品审评过程中残留溶剂检查常见问题分析
14.
Consideration for the guideline to the generic drugs development and review to meet the revised Drug Registration Regulation;
新版《药品注册管理办法》的实施对仿制药研发与技术评价要求的初步考虑
15.
Evolrement and Trend of the AppraisingProject of the Technology Innovation in China;
论我国技术创新项目评审的发展趋势
16.
FDA s Question-based Review: A Quality Assessment System for Generic Drugs;
FDA的仿制药品上市申请“问答式审评”质量评估体系简介
17.
Analysis and Inspiration of FDA CDER Sharing the Public Information Disclosure;
美国食品药品监督管理局药品审评和研究中心公众共享信息披露的分析和启示
18.
The quantitative check of academic thesis on evaluating technical or professional title;
专业技术职务评审中学术论文的量化考核