Ethical and trustworthy Artificial Intelligence

What medical device producers should know about the European Artificial Intelligence Draft Act (AIA)

December 22, 2023

1 Min Read
MDDI logo in a gray background | MDDI

Already have an account?

Additional regulation of AI-based Medical Devices (MDs) and In Vitro Diagnostics (IVDs) is progressing under the EU’s Artificial Intelligence Act (AIA). This paper explores this soon-to-be adopted regulatory framework as well as existing standards that will need to be harmonized, particularly for High Risk devices.

Sign up for the QMED & MD+DI Daily newsletter.

You May Also Like