EU Medical Device Regulation (MDR) - Updated CE Marking Process & ISO 13485:2016 Expectations

Name: EU Medical Device Regulation (MDR) - Updated CE Marking Process & ISO 13485:2016 Expectations
Start: 2022-06-01T10:00:00-07:00
End: 2022-06-01T11:30:00-07:00
Location: Live Webinar

Wed, Jun 01

Live Webinar

This EU Medical Device Regulation (MDR) 90-minute webinar will discuss the recently developed regulation and its impact on the future compliance and registration of medical devices in the EU.

Registration is closed

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