-2.png)
Qserve Group appoints Inette Nieveen-van de Laar to its Board of Directors, recognizing 11 years of leadership in medical device regulatory affairs.
-1.png)
Catch these five AI compliance gaps under EU MDR & IVDR early. What medtech software teams miss, and where to start fixing it.
-1.png)
Have non-EU clinical data? Learn what EU MDR actually requires for CE certification, and how to turn existing evidence into a defensible route to market.
-2.png)
Join Oliver Schaer and Bingshuo Li on 21-23 April at DMEA 2026 in Berlin and explore practical insights on Digital Health.
-2.png)
Join industry leaders, regulatory professionals and Qserve Expert Gert Bos at MedCon 2026 in Columbus, Ohio on Apil 22-24.
-1.png)
The transition to IVDR is entering its final phase, and the clock is ticking for Class C IVD manufacturers, as Notified Body assessment is now required.