Introduction

Overview: This Webinar will provide a substantive overview and outline differences between the Technical File and Design Dossier for those device firms dealing with the global regulatory landscape. It is assumed that participants and customers have a prior CE Mark and Medical Device Directive background. The Technical File is a comprehensive collection of information and documents that details everything about your medical device.

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• Further event details More information about the event

Venue

Online Training

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

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• Venue information More information about the venue

Organised by

GlobalCompliancePanel

Contact information

Online Training
United States of America
800-447-9407
Contact us by email

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