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UID:6a01ef335c5f2@www.leap-up.com
DTSTAMP:20260511T170107Z
DTSTART:20250401T113000
DTEND:20250402T170000
SUMMARY:Regulatory Affairs Expert Talks
DESCRIPTION:The medical technology industry in Germany is currently affected by various regulatory&nbsp\;challenges&nbsp\;that&nbsp\;exist at European and national level&nbsp\;. The regulatory landscape is complex and constantly changing. A lot has happened since the introduction of the Medical Device Regulation (MDR) in May 2021 and the increasing need for digital transformation&nbsp\;is bringing new challenges such as&nbsp\;artificial intelligence (AI)\, digitalisation and cybersecurity&nbsp\;increasingly into focus.\n\nExperts answer your questions\n\n\nAt the Regulatory Affairs Expert Talks you will meet experts who will explain what the new regulations mean for regulatory changes\, what this means for individual products and how the changes can be successfully implemented in companies.\n\n\nThe event is aimed at regulatory affairs managers\, quality managers and all those interested in regulatory affairs from medical technology companies.\n\nFurther information about the event can be found here.
LOCATION:Vogel Convention Center Würzburg\, Max-Planck Str. 7\, 97082 Würzburg
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