Introduction

This 90-minute webinar will provide valuable assistance to all regulated companies performing and documenting meaningful, results driven 510(k) / change analysis activities, based on the FDA's new Draft Guidance, "510(k) Device Modifications: Deciding When to Submit a 510(k) for a Change to an Existing Device", dated July 27, 2011.

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• Further event details More information about the event

Venue

Online Event

Online Event, 2600 E. Bayshore Road, Palo Alto, 94303, United States

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Organised by

ComplianceOnline

Contact information

Mr Referral
2600 E. Bayshore Road, Palo Alto, 94303, United States of America
+1-650-620-3915
Contact us by email

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