Introduction

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.

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• Further event details More information about the event

Venue

Online Event

Online Event, 161 Mission Falls Lane, Suite 216, Fremont, CA 94539, USA, Fremont, 94539, United States

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Organised by

GlobalCompliancePanel

Contact information

Mr John Robinson
161 Mission Falls Lane, Suite 216, Fremont, CA 94539, USA, Fremont, 94539, United States of America
08004479407
Contact us by email

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