14. January 2025
Prof. Dr. Boris Handorn
What’s changing in 2025: Life Science
For medical device manufacturers, the year 2025 begins with new information obligations in accordance with Art. 10a MDR. In contrast, urgently needed reforms to the MDR will continue to be evaluated in 2025. The life science sector will also be dominated by digitalization in 2025. In particular, topics relating to AI regulation in the medical device sector, flanked by data protection and data transparency, will come to the fore. Integration into the existing infrastructure in particular will play a central role.