Kevin Barber PhD, RAC, PMP

Kevin leads Syner-G’s Regulatory Consulting team, bringing over 30 years of expertise in product development and biomedical research. His team’s focus is on delivering value to clients by designing and executing effective regulatory strategies and clinical development plans that accelerate pathways to market and reduce time-to-value. With a proven track record of preparing over 100 INDs/CTAs and more than 80 marketing applications across key global markets, Kevin and his team ensure clients navigate complex regulatory landscapes efficiently and effectively.

In prior roles, Kevin has served as Senior Vice President of Regulatory Strategy & Submissions at Rho, Inc., where he played a pivotal role in scaling the global Integrated Product Development teams and driving significant business growth for regulatory and scientific consulting services. He also served as Vice President of Regulatory Affairs at Novan, Inc. and Vice President of Global Brand Regulatory Affairs at Actavis, Inc., responsible for regulatory product development for new products and regulatory life cycle management of approved products. Kevin holds a Master of Science in Aerospace Engineering from Virginia Tech and a PhD in Biomedical Engineering from Duke University.