EU Medical Device Regulation: Your Questions Answered
March 12, 2019 - Toronto ON CAXtalks
fbonilla@xtalks.com
Phone:1 416.977.6555
This webinar will address these and other critical questions and will pave the way to strategic planning for compliance with the EU MDR. New product development teams will discover that the timeline for MDR is extremely limited compared to existing products on the market. Post-market surveillance teams will discover the implications of the Post-Market Clinical Follow-up requirement and the European Database on Medical Devices.
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