Introduction

This webinar will discuss the new draft guidance document from the FDA: "510(k) Device Modifications: Deciding When to Submit a 510(k) for a Change to an Existing Device", dated July 27, 2011.

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Venue

Online Training

Online Training, 1000 N West Street,, Delaware, Suite 1200, Wilmington, 19801, United States

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Organised by

GlobalCompliancePanel

Contact information

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Online Training, 1000 N West Street, Suite 1200, Wilmington, 19801, United States of America
8004479407
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