This webinar will provide valuable assistance to all companies that market in the U.S., since they are by definition subject to FDA regulation, in the Medical Device, Diagnostic, Pharmaceutical, and Biologics fields.
How FDA Trains its Investigators to Review CAPA and What You Should Do to Prepare
10 August 2011, Wilmington, United States
Introduction
Venue
online training webinar
online training webinar, 1000 N West Street,, Suite 1200, Wilmington, 19801, United States
Useful links
Organised by
globalcompliancepanel
Contact information
Search
Advertisement
Spotlight
Explore
