Providing Regulatory, Quality, and Technical Medical Device Software Teams with Practical, Implementable Strategies for Designing and Validating Compliant, Competitive,
and Secure Devices
The 2nd Medical Device Software Development Summit Europe 2024
As device developers of all sizes grapples 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.
Our Expert Speakers Include:
Project Manager IVD Medical Device Testing & and Product Specialist
Senior Director, Medical Devices & Algorithms Software
Roche Diagnostics GmbH
Head of Regulatory Affairs, Software
What Have Past Attendees Found Most Valuable?
"The conference exceeded all my expectation. The diverse formats, and state-of-art topics were engaging and educational. I was extremely fortunate to have made the time to attend the full conference."
"The opportunity to share real-world experiences with others and to hear that we all have the same issues was incredibly helpful."
"A very interesting exploration of updates and changes to the software as a medical device landscape."