2nd Medical Device Software Development Europe 2024

R&D

As device developers of all sizes grapple with the updated transition timeline for EU MDR compliance and the recent EU AI Act approval falls short of expectations, the question looms: how can regulatory compliance align seamlessly with the pace of innovation?

Dedicated to shedding light on the intricate layers of European regulation, integrated cybersecurity features, and forecasted uncertainties around AI, the 2nd Medical Device Software Development Summit Europe serves as a pivotal platform to better align software innovation with compliance.

Join over 80 experts in Software Engineering, Regulatory Affairs, R&D Operations, Product Management, and more to harmonise cross-functional objectives and encourage an industry-wide push for more robust regulations that enable fast-paced innovations.

Learn More Here: https://ter.li/qivbna