James Smith

Smith boasts a wealth of expertise spanning more than fifteen years in regulatory affairs and the comprehensive lifecycle of pioneering technologies from inception to market launch. Proficient in regulatory affairs, quality assurance, data management systems, research and development oversight, formulation of new product specifications, and the assessment and registration of medical drug and device product portfolios. Dr. Smith earned his Ph.D. in Pharmacology and Toxicology from the University of California, Irvine.