Kevin Barber, Ph.D.

Vice President, Regulatory Strategy & Submissions

Kevin Barber

Kevin Barber, Ph.D.

Vice President, Regulatory Strategy & Submissions

Kevin Barber, PhD, RAC, PMP, serves as Rho’s Vice President of Regulatory Strategy & Submissions, providing extensive strategic leadership, scientific knowledge, and regulatory expertise to support Rho’s clientele in the development and execution of integrated regulatory strategies and clinical development plans for drugs, biologics, and medical devices. Dr. Barber has close to 25 years of experience in regulatory affairs and product development across all phases, from preclinical through product launch and post-approval life cycle management.  Dr. Barber holds a PhD in Biomedical Engineering from Duke University and prior to joining Rho, he served in leadership positions, including Senior Director of Regulatory Affairs and Project Management at a midsize global CRO, Vice President of Regulatory Affairs at a biotech startup, and Vice President of Global Brand Regulatory Affairs at a midsize pharmaceutical company.  He has significant experience moderating regulatory authority meetings and preparing and filing regulatory submissions, including more than 40 US INDs and more than 40 marketing applications in the US, Canada, Europe, and other regions.