This webinar is intended to share 510(k) hurdles and good practices, in particular, how to prepare a 510(k) in a sufficiently adequate manner with increased quality to expedite review process. The premarket notification [510(k)] is the most common pathway to market for medical devices including in vitro diagnostic medical devices.
Update on FDA 510(k) Review Process, Hurdles and Good Practices on 510(k) Preparation and Clearance
17 July 2014, Fremont, United States
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Venue
Online Event
Online Event, 161 Mission Falls Lane, Suite 216, Fremont, CA 94539, USA, Fremont, 94539, United States
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GlobalCompliancePanel
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