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.
Construct and Manage the Technical File and Design Dossier
16 July 2013, United States
Introduction
Venue
Online Webinar
Online Webinar, United States
Useful links
Organised by
Compliance Trainings
Contact information
Ms Anita Anzo
416-915-4458
416-915-4458
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