Bill Gannon Jr., MD, MBA

Bill has spent the last 20 years in the development, regulatory – NDA, BLA, ANDA, IND, IDE, PMA and 510K FDA submissions and approvals, commercialization, marketing and management of products and technologies for the healthcare, medical devices, allied health and pharmaceutical industries. He is also well versed with the European (ISO 9000), Canadian and Japanese regulatory environments, and with IBC AHA and JCAHO regulatory affairs processes.