LCDR Lisa Kwok, Pharm. D.
Lisa Kwok is a Senior Regulatory Project Manager in the Office of Generic Drugs, Food and Drug Administration. She serves as the primary liaison between FDA and Industry and monitors the overall application review process of generic drugs. LCDR Kwok received her Doctor of Pharmacy from the University of the Sciences in Philadelphia, Philadelphia College of Pharmacy in 2002 and is currently pursuing a Masters in Public Health with a concentration in Emergency Management from the American Military University. Before joining the FDA, LCDR Kwok worked in a retail chain pharmacy for 3 years.