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Terry Layton, Ph.D.

Dr. Terry Layton has 40 years of experience in the medical device industry. He is a technical executive with strong background in building medical device manufacturing companies. His diverse experience includes industry and consulting work in product development, regulatory/QA, operations, IP, failure investigation, technology assessment, mergers and acquisitions, and licensing of medical devices.

He is an instructor and lecturer for bioentrepreneur classes and seminars on medical device design, ISO & GMP regulations, product development, emerging medical technologies and medical device commercialization. His classes and seminars emphasize medical device industry skill sets.

In addition, Layton is a past or present member of FDA Advisory Panels (Anesthesia, General Hospital, and Gastroenterology and Urology), NIH Technology Review, Networks of Centres of Excellence (Canada), and Kentucky Science & Technology Corporation.


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