Eric Mui

Eric Mui, PharmD, RPh, RAC, is an experienced regulatory affairs professional currently serving as the Associate Director of Biopharm CMC Regulatory Affairs at GSK. With over 14 years in the pharmaceutical industry, Eric has expertise in Chemistry, Manufacturing, and Controls (CMC) Regulatory Affairs, as well as in cGMP quality control and analytical laboratory functions. Previously, Eric held multiple roles at PPD, advanced through various positions at GSK from Associate to Manager, and contributed as a Postdoctoral Fellow at the University of North Carolina at Chapel Hill. Eric's educational background includes a Doctor of Pharmacy (Pharm.D.) from the University of Wisconsin-Madison and a Postdoctoral Fellowship in Regulatory Affairs from the same institution.