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UID:69e4b7d197a9b@leapup.bitshifters.cloud
DTSTAMP:20260419T130905Z
DTSTART:20250429T084500Z
DTEND:20250429T130000Z
SUMMARY:PMS compact: Your practical guide to post-market surveillance
DESCRIPTION:The European Medical Device Regulation (MDR) requires medical device manufacturers to conduct post-market surveillance (PMS). The aim of 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.
LOCATION:MS Teams\, Offenbach am Main
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