Peggy Hansen joined Regenity in October 2001. Peggy has 25 years of experience in regulatory affairs, clinical research, and quality assurance of implantable medical devices and over 12 years in business development and marketing for Regenity.
Before joining Regenity, Peggy was the Manager of Regulatory Affairs at SurModics, Inc., a company specializing in surface modification of medical devices, where she was responsible for the company’s regulatory affairs and quality compliance. Prior to working at SurModics, Peggy was at 3M Health Care, Medical Products Division and Cardiovascular Systems Division where she was responsible for U.S. and global regulatory filings with respect to the company’s class I, II, and III medical devices and combination products. Peggy was also employed by ReGen Biologics, Inc., a company involved in the development of collagen orthopedic products. She is a certified Regulatory Affairs Professional.
She received her Bachelor’s degree in Chemical Engineering from Cornell University.
I value the interactions we have with our clients, being part of their team and helping them further their vision and mission. We are grateful for several long-term relationships we’ve established based on our commitment, expertise, regulatory acumen and quality products.
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