Carrie Hetrick

Carrie Hetrick

Director of Regulatory and Clinical Affairs
Sterling Medical Devices

Categories covered by Carrie

About this Speaker

Carrie Hetrick leads the regulatory, clinical, and quality programs at Sterling Medical Devices, helping companies navigate challenges in product development while establishing appropriate clinical, regulatory, and compliance structures during each stage of development. Dr. Hetrick has been involved in medical technology for over 25 years, focusing on the intersection of technology, regulation, and health care and has led numerous quality management and business process improvement/ management measures. A seasoned subject matter expert in taking new products from R&D to market, she has used her regulatory and clinical expertise to aid in hundreds of successful regulatory submissions and clinical trials in the U.S. and Europe. Dr. Hetrick has led numerous quality management and business process improvement and management measures. She is also experienced in leading early and late-stage cross-functional medical product development programs, directing activities and teams for all phases of design controls, and creating collaborative alliances. She holds a Master of Science in Advanced Biotechnology, Regulatory Science from Johns Hopkins University, a Doctor of Dental Surgery from the University of Colorado Health Science Center School of Dentistry, and a Bachelor of Science in Biology from Pacific Lutheran University. She finds great reward in helping patients through ushering products to market.

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