Welcome to the 2nd Medical Device Software Development Summit Europe, the definitive conference for practical answers with real-world evidence and case studies.
Welcome to the 2nd Medical Device Software Development Summit Europe, dedicated to spotlighting case studies in better aligning innovative software development, device security, and regulatory compliance.
Whether you’re a first-timer or a returning participant, immerse yourself in illuminating the intricacies and current challenges of the medical device software domain. Join industry thought leaders, ranging from established device developers to innovative start-ups, to share practical insights in overcoming the regulatory bottleneck in innovation, delineate a matrix of country-specific regulations, and align cross-functionally to streamline software development.
This unique platform offers a comprehensive exploration of both the hottest topics and industry bottlenecks, including:
Exploring cutting-edge strategies for crafting a robust product framework, featuring engaging presentations and discussion on key pillars such as cybersecurity, post-market surveillance, and risk management, led by leading experts from Roche, Straumann Group BD, and more
Gain profound insights into the regulatory and technical aspects of Artificial Intelligence, including a comprehensive presentation of the AI Act, with groundbreaking insights from 3Shape
Successfully navigate the complex landscape of medical device regulations, ensuring a seamless and compliant journey throughout your product development process, with valuable learnings and insights from TÜV SÜD, Johnson & Johnson, InnoCon Medical, and others
Exploring strategic pathways for entering the US market successfully by incorporating dual compliance demands and gaining insights into FDA requirements with key learnings from Novo Nordisk