Headline EU-MDR & Software as a Medical Device

The FDA and EU-MDR are constantly tightening the compliance regulations for Medical Devices, spawning a completely new set of extensive requirements that have the potential to cause disruptions for suppliers of medical Software. 

In this webinar, Prof. Dr. Christian Johner (Johner Institute) and Steffen Rehnig (Principal Consultant Software Monetization, Thales DIS) demonstrate and discuss:

  • The relevant changes and what they mean for manufacturers of classified software and devices.
  • Valuable suggestions on how manufacturers can meet the new requirements. 
  • How to avoid compliance problems with software licensing. 
  • How digital transformation can benefit from software licensing.

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