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 what it takes to successfully navigate the certification process from a Notified Body perspective.\nAs MDR requirements continue to evolve\, medical device manufacturers are facing increasing challenges in aligning their quality systems and technical documentation with regulatory expectations. In this webinar\, we will share practical insights into the certification process\, highlight common challenges observed during assessments\, and discuss how to better prepare for a smooth and efficient MDR journey.\nHosted by UDEM Atlantic\, the U.S. office of European Notified Body 2292\, this session will provide a clear overview of how manufacturers can approach MDR certification with confidence and clarity.\nKey topics will include:Overview of the EU MDR certification processExpectations from a Notified Body perspectiveCommon challenges in documentation and QMS readinessPractical considerations for a successful certification pathwayWhether you are preparing for MDR certification or evaluating your next steps\, this session will offer valuable guidance to support your regulatory strategy.\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 what it takes to successfully navigate the certification process from a Notified Body perspective.


As MDR requirements continue to evolve\, medical device manufacturers are facing increasing challenges in aligning their quality systems and technical documentation with regulatory expectations. In this webinar\, we will share practical insights into the certification process\, highlight common challenges observed during assessments\, and discuss how to better prepare for a smooth and efficient MDR journey.


Hosted by UDEM Atlantic\, the U.S. office of European Notified Body 2292\, this session will provide a clear overview of how manufacturers can approach MDR certification with confidence and clarity.


Key topics will include:

Whether you are preparing for MDR certification or evaluating your next steps\, this session will offer valuable guidance to support your regulatory strategy.


Register here: \;

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





LOCATION:Medford MA 02155 UID:e.1244.1428398 SEQUENCE:3 DTSTAMP:20260406T200410Z URL:https://business.massmedic.com/events/Details/udem-atlantic-eu-mdr-in-practice-insights-from-a-notified-body-perspective-1689773?sourceTypeId=Hub END:VEVENT END:VCALENDAR