A regulatory and quality compliance Professional with experience in all four corners of rapid product development, clinical study, Quality System compliance, and regulatory approval of innovative high quality Class II and III medical devices. I have a record of demonstrated success and possess the particular set of skills and experience needed to develop compliant systems and bring new medical products to market in the shortest time possible. He also serves as an Adjunct Professor at the University of Minnesota instructing a 4000 level course and a Graduate level course on medical device development and is also a Faculty Director within the College of Continuing and Professional Studies. Specialties Committee and board members; AdvaMed and Medical Alley, RAPS, Xavier Health, MDIC • Actively engaged with FDA leadership and state legislators advocating efficient and effective pathways to develop innovative and safe products. Holds a BS in Industrial Technology from Iowa State University and an MBA from the University of Dallas and is RAC certified and elected as a RAPS Fellow, FRAPS.