BEGIN:VCALENDAR VERSION:2.0 PRODID:-//ChamberMaster//Event Calendar 2.0//EN METHOD:PUBLISH X-PUBLISHED-TTL:P1H REFRESH-INTERVAL:P1H CALSCALE:GREGORIAN BEGIN:VTIMEZONE TZID:America/New_York BEGIN:DAYLIGHT RRULE:FREQ=YEARLY;BYMONTH=3;BYDAY=2SU DTSTART:20070101T000000 TZOFFSETFROM:-0500 TZOFFSETTO:-0400 TZNAME:Eastern Daylight Time END:DAYLIGHT BEGIN:STANDARD RRULE:FREQ=YEARLY;BYMONTH=11;BYDAY=1SU DTSTART:20070101T000000 TZOFFSETFROM:-0400 TZOFFSETTO:-0500 TZNAME:Eastern Standard Time END:STANDARD END:VTIMEZONE BEGIN:VEVENT DTSTART;TZID=America/New_York:20260428T100000 DTEND;TZID=America/New_York:20260428T110000 X-MICROSOFT-CDO-ALLDAYEVENT:FALSE SUMMARY:Udem Atlantic- EU MDR in Practice: Insights from a Notified Body Perspective DESCRIPTION:Join us for an insightful session on EU MDR and how to successfully navigate the certification process combining Notified Body expertise with hands-on technical documentation insights.\nAs MDR requirements continue to evolve\, medical device manufacturers face increasing challenges in aligning their technical documentation\, clinical evidence\, and quality systems with regulatory expectations.In this session\, we will share practical insights from a Notified Body perspective\, along with real-world approaches to technical documentation and post-market surveillance (PMS) helping you better prepare for a smoother and more efficient MDR journey.\nHosted by UDEM Atlantic\, the U.S. office of European Notified Body 2292\, this webinar brings together expertise in:Key topics will include:Overview of the EU MDR certification processNotified Body expectations during assessmentsCommon gaps in clinical evidence and documentationHow to structure technical documentation to reduce delaysPractical insights into Post-Market Surveillance (PMS)Whether you are preparing for MDR certification or optimizing your current strategy\, this session will provide actionable insights to support your next steps.\nRegister here: https://events.zoom.us/ev/AlGaC3dSvEnuNm_OAR-5zVcDz5foKu7kVLCVyvR0bjuMkpftsYbZ~ApgFQNy6rMmQ3AbNlIMND_H0W6b1q0tikwstB_NEIJznmN39NnAof-R7jQ X-ALT-DESC;FMTTYPE=text/html:


Join us for an insightful session on EU MDR and how to successfully navigate the certification process &mdash\; combining Notified Body expertise with hands-on technical documentation insights.


As MDR requirements continue to evolve\, medical device manufacturers face increasing challenges in aligning their technical documentation\, clinical evidence\, and quality systems with regulatory expectations.

In this session\, we will share practical insights from a Notified Body perspective\, along with real-world approaches to technical documentation and post-market surveillance (PMS) &mdash\; helping you better prepare for a smoother and more efficient MDR journey.


Hosted by UDEM Atlantic\, the U.S. office of European Notified Body 2292\, this webinar brings together expertise in:

Key topics will include:

Whether you are preparing for MDR certification or optimizing your current strategy\, this session will provide actionable insights to support your next steps.


Register here: \;

https://events.zoom.us/ev/AlGaC3dSvEnuNm_OAR-5zVcDz5foKu7kVLCVyvR0bjuMkpftsYbZ~ApgFQNy6rMmQ3AbNlIMND_H0W6b1q0tikwstB_NEIJznmN39NnAof-R7jQ




LOCATION: UID:e.1244.1428398 SEQUENCE:3 DTSTAMP:20260417T180340Z URL:https://massmedic.growthzoneapp.com/events/Details/udem-atlantic-eu-mdr-in-practice-insights-from-a-notified-body-perspective-1689773?sourceTypeId=Hub END:VEVENT END:VCALENDAR