Education
•B.S., Physics, Peking University
•M.S., Physics, Chinese Academy of Sciences
•Ph.D., Physics, Temple University
Research Areas
Regulatory science with a focus on pharmaceutical quality regulation, characterization and communication of pharmaceutical quality, knowledge engineering and evaluation
Teaching Courses
- Regulation of pharmaceutical products
- Pharmaceutical quality and global health
Selected Publications (* indicates the corresponding author)
- Economic Impacts of the Generic Drug User Fee Act Fee Structure, K. Dong, G.Boehm, Q.Zheng*, Value in Health, 20(6) 792-798, 2017
- Factors to consider in developing individual pharmaceutical product quality risk profiles useful to government procurement, W.Xu, G.Boehm, Q.Zheng*, Acta Pharmaceutica Sinica B 6(1) 79-92, 2016
- (In Chinese) J.Dai and Q.Zheng*, Application of Statistics Methodology in Pharmaceutical R&D, Manufacturing and Quality Management, Chinese Journal of New Drugs 23(9) 1024, 2014
- G.Boehm, L.Yao, L.Han and Q.Zheng*, Development of the Generic Drug Industry in the US after the Hatch-Waxman Act of 1984, Acta Pharmaceutica Sinica B. 3(5), 297, 2013
- (In Chinese) Q.Zheng* (Executive Editor), Guidance of Good Manufacturing Practice for Drugs (Six Volumes), China Medical Science Press, 2012