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 and 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.

Prices:
Drug Developer Pricing - Conference + 3 Workshops: EUR 4296.00,
Drug Developer Pricing - Conference + 2 Workshops: EUR 3797.00,
Drug Developer Pricing - Conference + Workshop: EUR 3298.00,
Drug Developer Pricing - Conference Only: EUR 2799.00,
Vendor Pricing - Conference + 3 Workshops: EUR 5196.00,
Vendor Pricing - Conference + 2 Workshops: EUR 4597.00,
Vendor Pricing - Conference + Workshop: EUR 3998.00,
Vendor Pricing - Conference Only: EUR 3399.00,
Academic Pricing - Conference + 3 Workshops: EUR 3596.00,
Academic Pricing - Conference Only: EUR 2399.00

Speakers: Alexander Stock, Project Manager IVD Medical Device Testing and and Product Specialist, TUV SUD, Andreia Pimenta, Clinical Evaluation and Surveillance Manager, Ada Health, Christian Jensen, Product Reviewer, TUV SUD, Dr. Shaloo Sood, Team Leader RDI Academy, Institut Straumann, Emmett Farrell, Regulatory Affairs Manager, Ypsomed, Fariborz Karimi, Regulatory Affairs Specialist, Johnson and Johnson Services, Inc, Francois Peter, Senior Director of Software Engineering, GE Healthcare, Igor Menghini, Senior Director, Medical Devices and Algorithms Software, Roche Diagnostics GmbH, Jean Chaoui, Vice President of Clinical Applications and Solutions, Digital, Robotics and Enabling Technologies, Stryker Corp., Lionel Marty, Senior Manager, Software As Medical Device Technology Lead, Biogen, Lukas Futera, Principal Cyber Security Architect, Roche Diagnostics GmbH, Mette Luxhoj, Head of Regulatory Affairs, Software, 3Shape A/S, Morten Cramer, Head of HW/SW, InnoCon Medical, Oscar Tonelli, Lead Systems Engineer, Novo Nordisk, Paul Fletcher-Dyer, Artificial intelligence Compliance Director and Data Protection Officer, Cognetivity Neurosciences, Paula Antunes, Global Regulatory Lead, Novo Nordisk, Tauseef Mehrali, Vice President of Medical Safety and Regulatory Affairs, Ada Health, Robert Krejci, Senior Manager, Software Engineering, BD Technologies

Others Details

Brochure: https://go.evvnt.com/2007133-3?pid=6581