Faculty

Dr. Tee Khim Boon is a Senior Principal Assistant Director at Malaysia’s National Pharmaceutical Regulatory Agency (NPRA). With over 18 years of regulatory experience, she is a leading authority on clinical trial evaluations (Phase I–III), overseeing import and exemption licenses with rigorous scientific oversight. 

A University of Malaya PhD graduate, Dr. Tee has been instrumental in shaping Malaysia’s clinical research landscape. She has spearheaded the development of national clinical trial laws, regulations, and the Malaysian Guideline for Good Clinical Practice.

Her expertise extends to conducting international and domestic inspections of clinical trial sites, bioequivalence centers, and ethics committees. Through her leadership, Dr. Tee ensures the highest ethical standards, safeguarding public health while advancing robust investigational medicinal product regulation.