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.
Construct and Manage the Technical File and Design Dossier - Webinar By GlobalCompliancePanel
17 July 2012, United States
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Online Training
Online Training, 1000 N West Street, Suite 1200, 19801, United States
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GlobalCompliancePanel
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