Introduction

Major postmarketing vigilance revisions are now in force. A revised medical device guidance document on postmarketing vigilance (MEDDEV 2.12-1 rev 5) came into force on January 1, 2008. Providing more guidance than the previous version, the new document includes new reporting terminology and concepts such as "periodic summary reporting" and "trend reporting."

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Venue

Online Training

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

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Organised by

GlobalCompliancePanel

Contact information

Online Training
United States of America
800-447-9407
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