This webinar is intended to demonstrate how to prepare a 510(k) in an adequate manner with increased quality to expedite the streamlined review process. The premarket notification [510(k)] is the most common pathway to market for medical devices including in vitro diagnostic medical devices.
510(k): Format and Contents - Webinar By GlobalCompliancePanel
10 April 2013, Fremont, United States
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Online Training
Livermore Common, Online Training, California, Fremont, 94539, United States
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GlobalCompliancePanel
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