Course at Cranfield University Dedicated to US Regulation of Medical Technology

Scheduled for February 24–26, a course developed by Cranfield University in collaboration with TOPRA will examine how US regulatory procedures are applied to medical technologies. Offered by Cranfield University in the United Kingdom, the course is designed to enable attendees to leave with the capability to advise their organizations about entering the US medical technologies market. It will focus on such areas as the structure and mission of the US FDA, pre-market notification, and quality system regulation. A master of science program in medical technology regulatory affairs is also offered by the university.

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Tags: Cranfield University, regulatory standards, TOPRA, US FDA