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UID:6a796e101c719@www.leap-up.com
DTSTAMP:20260810T082208Z
DTSTART:20250429T084500
DTEND:20250429T130000
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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