Date & Time
- from
- 01/04/2025
- until
- 02/04/2025
- duration
- 1day
The medical technology industry in Germany is currently affected by various regulatory challenges that exist at European and national level . 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 is bringing new challenges such as artificial intelligence (AI), digitalisation and cybersecurity increasingly into focus.
Experts answer your questions
At 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.
The event is aimed at regulatory affairs managers, quality managers and all those interested in regulatory affairs from medical technology companies.
Further information about the event can be found here.
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