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DESCRIPTION:This webinar will help you understand the requirements of the 
 new medical device regulation EU MDR 745/2017 and teach you how to create
  new required reports for the Notified Body and the Competent Authorities
  and how this process is connected to other processes in the quality mana
 gement system according EN ISO 13485:2021.\n\nWhy Should You Attend:\n\nY
 ou should attend this webinar to understand\, what are the changes to the
  previous medical device regulation and how to implement the changes in y
 our current quality management system according ISO 13485:2021 like post-
 market-surveillance plan and report and how to create the annual PSUR – P
 erformance Safety Update Report to the Notified Bodies and EUDAMED in a s
 imple and quick way. Your implementation need smart ideas to reach the ri
 ght level to pass the quality management audit by your certification comp
 any or notified body.\n\nAreas Covered in the Webinar:\n\n\nHow to define
  a “Post-Market-Surveillance-Process”?\nHow to create the new required re
 ports for the Notified Body and the Competent Authorities?\nHow to do adj
 ustments in the management review\nHow is the Post-Market-Surveillance-Pr
 ocess” connected to clinical evaluation\, customer feedback\, complaints 
 and vigilance?\n\nWho Will Benefit:\n\nCEO’s\, product manager\, quality/
  regulatory / medical affairs manager\, quality representatives of\n\n\nm
 edical device manufacturers\nimporter\ndistributors\ndealers\n\nwho work 
 with European Union\, European Economic Area\, Switzerland and Turkey\n
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DTSTAMP:20260512T232624Z
DTSTART:20250505T100000
LOCATION:\,
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SUMMARY:This webinar will help you understand the requirements of the new 
 medical device regulation EU MDR 745/2017 and teach you how to create new
  require...
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