Introduction

Medical Device Reporting (MDR) is the mechanism for the Food and Drug Administration to receive significant medical device adverse events from manufacturers, importers and user facilities, so they can be detected and corrected quickly.

Price: $225.00

GlobalCompliancePanel
Phone: 800-447-9407
webinars@globalcompliancepanel.com

http://bit.ly/QrDZVM

Useful links

• Further event details More information about the event

Venue

Online Training

Livermore Common, Online Training, Fremont, CA, 94539, United States

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• Venue information More information about the venue

Organised by

GlobalCompliancePanel

Contact information

Mr John Robinson
Fremont, 94539, United States of America
8004479407
Contact us by email

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