Medical device software process design: why IEC 62304 matters
How confident are you that your medical device software processes could withstand a regulatory ...
Author Aurevia:
Streamline your clinical study application
Regulatory requirements are becoming increasingly complex, and managing submissions, amendments, ...
MD software process design course: 25-26 November
Do you work with medical device software process design? Together with Intertek Academy, we offer a ...
European Society For Medical Oncology (ESMO) Congress: 23-27 October
Aurevia will participate in the ESMO Congress, taking place on 23–27 October 2026 in Madrid, Spain. ...
CCLs: Bridging science and practice
At Aurevia, we have experienced Clinical Country Liaisons (CCLs), a role that shares many ...
Health Design: 28-29 October
See you at Health Design in Helsinki and Espoo on 28-29 October! We’re excited to attend Health ...
Medical devices for beginners: 20-21 October
We're excited that Kirsten Sander, from Aurevia GmbH, will be speaking at the Medizinprodukte für ...
CTIS updates
The Clinical Trials Information System (CTIS) has introduced several updates aimed at improving ...
The Three Pillars of Clinical Evidence Under the IVDR
The IVDR raises the bar. Many in vitro diagnostic (IVD) medical device manufacturers still ...