This webinar will discuss FDA concerns in medical device safety expressed in reports on 510(k) products.
The 510(k) Process and Risk Management - Webinar By GlobalCompliancePanel
8 September 2011, Wilmington, United States
Introduction
Venue
online training webinar
online training webinar, 1000 N West Street, Suite 1200, Wilmington, 19801, United States
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Organised by
globalcompliancepanel
Contact information
Mr webinar web
online training webinar, 1000 N West Street, Suite 1200, Wilmington, Zip 19801, United States of America
18004479407
Contact us by email
online training webinar, 1000 N West Street, Suite 1200, Wilmington, Zip 19801, United States of America
18004479407
Contact us by email
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