James Smith
Regulatory Affairs/Quality Assurance Advisor
Healthcare Experts
Leardon Solutions
Spain
Biography
Dr. Smith has over fifteen years of experience in regulatory affairs and the development of novel technologies from concept through commercialization. He is experienced in all aspects of regulatory affairs, quality and data management systems, supervision of R&D, development of new product specifications, and with evaluating and registering medical drug and device product lines. Dr. Smith obtained his Ph.D. in Pharmacology and Toxicology from the University of California, Irvine.
Research Interest
medical drugs
