MingPing Zhang

MingPing Zhang

MingPing Zhang

Vice President, Technical

Mingping is responsible for providing clients with regulatory and Chemistry, Manufacturing, and Controls (CMC) consulting for the Asia Pacific region, especially China.

Work Experience

Prior to joining Parexel, Mingping spent five years working in the pharmaceutical industry as a CMC Director at BeiGene (Beijing) Co.,Ltd. and Regulatory CMC manager at Novartis. His responsibilities have included drafting, reviewing and finalizing the China & US submission documents (CMC part), generating and maintaining CTA and NDA CMC template for China submission; and acting as a core member of China development strategy work stream in Novartis. Mingping also has six years’ experience as a CMC reviewer at CDE of CFDA. In his time there he: evaluated tens of innovative drugs and international multi-centered clinical trial drug applications(cardiovascular agents; blood system agents, electrolyte/acid-base balance/ nutrition agents, antibiotic, gynecologic agents and antidepressants and anti-cancer drugs); reviewed over 1,000 IND, NDA, ANDA and Supplementary applications; became familiar with most of the advance technology of pharmaceutical industry; such as fermentation, solid phase peptide synthesis, biological Purification, chiral synthesis, liposome, micelle, solid dispersion, emulsion, control release system etc; and audited over twenty pharmaceutical factories. Minpging is fluent in English and Chinese (dialects: Cantonese and Teochew).


Mingping has a Bachelor’s degree in engineering from Beijing University of Chemical Technology and a Master’s degree in chemical engineering (control release) from the National University of Singapore

Connect With Me

We are always available for a conversation.