Book Online Tickets for  EU Medical Device Regulation (MDR) Upda, Palo Alto. 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. It includes specific insights from direct involvement and

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

 

  • One Dial-in One Attendee

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    USD 229
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  • Group-Max 10 Attendees or Location

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  • 1x Person - Unlimited viewing for 6 Months

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    USD 299
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  • One CD and USB is for usage in one location only

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    USD 399
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  • Live + Recorded Version

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  • Live + Training CD or USB

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    USD 499
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About The Event

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. It includes specific insights from direct involvement and work within the EU and the Commission's major improvement objectives to their system today. Areas of change between the prior Medical Device Directive (MDD) and the MDR will be discussed as well as expectations for how to implement ISO-13485:2016.