Carole C. Carey

2003-2005

9

Maryland

U.S. Department of Health and Human Services, U.S. Food and Drug Administration

Ministry of Health, Labour and Welfare

Gain knowledge of Japan’s pre-market requirements and the review process for medical devices. Learn about post-marketing studies and surveillance safety programs for medical devices in order to gain insight into how Japan’s pre-market, post-market and enforcement divisions exchange information.