Dr. Manberg has four decades of experience leading the regulatory and clinical development programs for a wide range of medical device and pharmaceutical products. He has designed and executed numerous US and international multicenter clinical trials leading to successful product registrations and market adoption activities while holding executive positions at Ares-Serono, Aspect Medical Systems, Covidien, CSA Medical and Health Data Analytics Institute. Since 2011, Dr. Manberg has maintained an active clinical and regulatory strategic consulting practice for early-stage medical industry clients. He received his BS degree in Biology from SUNY-Binghamton and his Ph.D. in Pharmacology from the University of North Carolina School of Medicine.
Dr. Paul Manberg