Nancy So

Nancy So is a Principal Regulatory Affairs Specialist at Boston Scientific, bringing over five years of experience in regulatory affairs, particularly in high-risk medical device submissions. They have successfully led Canadian and international submissions, focusing on product lifecycle management and ensuring compliance with various regulatory standards. Their expertise extends from consulting in start-up environments to managing multidisciplinary teams in established companies. With a Ph.D. in Molecular Genetics from the University of Toronto, Nancy is passionate about the regulatory process that brings therapeutics from discovery to patient care.