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UID:69e4b12e99375@leapup.bitshifters.cloud
DTSTAMP:20260419T124046Z
DTSTART:20240910T084500Z
DTEND:20240910T160000Z
SUMMARY:Post-market compliance - efficient implementation of PMS\, PMCF and vigilance
DESCRIPTION:The European Medical Device Regulation (MDR) obliges medical device manufacturers to perform post-market surveillance (PMS) and post-market clinical follow-up (PMCF). The corresponding processes in the quality management system (QMS) play a central role in ensuring safety and performance over the entire life cycle of medical devices.\nThe aim of the PMS is to identify potential risks or undesirable events that occur during the use of a medical device and to take appropriate measures to protect users. Closely related to this is the topic of vigilance and the associated reporting obligations for manufacturers.
LOCATION:MS Teams\, Offenbach
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