top of page

Wed, Jun 01

|

Live Webinar

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

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

Time & Location

Jun 01, 2022, 10:00 AM – 11:30 AM PDT

Live Webinar

Share this event

bottom of page