Introduction

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. Understanding how to assemble this information and present the information properly is essential.

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• Further event details More information about the event

Venue

Online Webinar

Online Webinar, United States

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Organised by

Compliance Trainings

Contact information

Ms Anita Anzo
416-915-4458

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