Kristine Canavan

Kristine Canavan is an experienced regulatory professional with a wealth of medical device and combination product experience. A Biomedical engineer by training, with an MPH in Biostatistics and Epidemiology, she has over 25 years of industry experience including several executive positions in regulatory, quality and clinical. She has actively managed products to market from early-stage product development efforts through the regulatory submissions and post-market activities. Kristine has held with Medtronic, Covidien and DePuy, in addition to several successful start-up companies.