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郑强

 

郑强

 
 
 

博士、教授


北京大学药物信息与工程研究中心主任


联系电话:010-6275-6142
电子邮箱:zhengqiang@pku.edu.cn 
个人主页:http://www2.coe.pku.edu.cn/subpage.asp?id=121


郑强
 

 

教育经历:


•B.S., Physics, Peking University
•M.S., Physics, Academia Sinica
•Ph.D., Physics, Temple University
 

研究领域:


Quantitative characterization of the quality management systems of pharmaceuticals and biologics.  
 

背景资料:

Dr. Qiang Zheng is Professor with Department of Industry Engineering and Management of College of Engineering, and Director of Center for Pharmaceutical Information and Engineering Research, Peking University. He is also Director of the Master's Degree Program in International Pharmaceutical Engineering Management, which is a collaboration program between Peking University and the US FDA. He teaches pharmaceutical quality and global health at Peking University.
Dr. Zheng’s research focuses on quantitative characterization of the quality management systems of pharmaceuticals and biologics. Recently, he led a team of 150 people from 50 organizations to draft the guidances for SFDA's new GMP regulation. Currently, He is developing a mathematical model and database system to measure the quality risks of pharmaceutical manufacturing for the SFDA.  
Dr. Zheng has studied quantitative modeling of biological and medical systems for over two decades, with over thirty peer-reviewed scientific publications and an international patent. Dr. Zheng received his BS, MS and PhD in Physics from Peking University and Academia Sinica in China and Temple University in the US, respectively. 
 
北京大学工学院工业工程与管理系教授,北京大学药物信息与工程研究中心主任。 还任北京大学国际药物工程管理硕士项目负责人,该项目是北京大学和美国FDA的合作项目。在北京大学讲授药品质量与全球健康的课程。
 
研究兴趣在药品和生物制品质量管理体系的量化特征及应用。最近,领导了50余家单位的150余人为国家药监局认证中心起草了新版GMP的指南,约2200页,150万字。目前,为国家药监局研制药物生产质量风险量化模型。
 
从事生物和医药系统的应用型量化研究20余年,发表了30篇同行审评的科学文章,获得一项国际专利。曾分别在北京大学、中国科学院和美国Temple大学获得物理学学士、硕士和博士学位。