— Daniel Schultz, commenting on the FDA's increased emphasis on post-approval surveillance, CDRH's Schultz outlines his 2008 action plan for agency," pp. 1, 5.
All Clarivate websites use cookies to improve your online experience. They were placed on your computer when you launched this website. You can change your cookie settings through your browser.
Subscribe to BioWorld™ news services
— Daniel Schultz, commenting on the FDA's increased emphasis on post-approval surveillance, CDRH's Schultz outlines his 2008 action plan for agency," pp. 1, 5.