A premarket notification [510(k)] submission is the most common pathway to market for medical devices including in vitro diagnostic devices.
510(k) Submissions: Requirements, Challenges and Successful Clearance - Webinar By GlobalCompliancePanel
19 April 2012, Wilmington, United States
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OnlineTraining
OnlineTraining, 1000 N West Street, Delaware, Suite 1200, Wilmington, 19801, United States
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Online Training, 1000 N West Street, Suite 1200, Wilmington, 19801, United States of America
8004479407
Contact us by email
Online Training, 1000 N West Street, Suite 1200, Wilmington, 19801, United States of America
8004479407
Contact us by email
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