Mr. Winegar's primary focus is in the areas of medical device regulatory affairs, clinical research, and quality assurance. He has more than thirty years of experience with global medical device and biotechnology companies, with a particular emphasis on neurovascular, cardiovascular, peripheral vascular, and regenerative medicine technologies. Mike has held senior leadership positions with a number of large and small medical device companies, as well as providing consulting services to medical device and biotechnology companies.
Program Director of M.S. in Regulatory Science
Regulatory Science & Medical Device Development
BS, Microbiology, University of Minnesota, College of Biological Sciences, 1982.
- Medical Device Startups, Cellular Therapies, First-In-Human Clinical Trials, Medical Device Sterilization, Biocompatibility Testing.
- Research Interests
- His current interests include start-up medical device and biotechnology ventures, specifically in the cardiovascular and regenerative medicine areas.