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UID:6a3ba1cab3dfd@www.leap-up.com
DTSTAMP:20260624T112218Z
DTSTART:20250430T084500
DTEND:20250430T130000
SUMMARY:Vigilance in action: from mandatory reporting to hazard prevention
DESCRIPTION:The European Medical Device Regulation (MDR) requires medical device manufacturers to ensure vigilance. The MDR stipulates that incidents in connection with medical devices must be recorded and evaluated by the manufacturer and\, if necessary\, reported to the national competent authorities. This is intended to ensure and improve the health protection and safety of patients\, users and third parties.
LOCATION:MS Teams\, Offenbach am Main
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