
Expert Insights, Tailored Networking, and Cutting-Edge Solutions Designed for Professionals Like You
MedTech Summit 2026 is the ultimate event for consultants and advisory professionals in the medtech industry. Check in with your existing community of regulatory leaders, meet new clients through the ConnectMe platform, and stay informed about the latest challenges facing manufacturers.
Network with key stakeholders, including manufacturers, notified bodies, and regulatory authorities, and explore tracks tailored to your expertise, such as EU MDR, SaMD & AI, and Clinical & PMS. Join roundtable discussions to gain deeper insights and actionable takeaways.
Customised Programmes to Drive Innovation and Success
European Regulatory Affairs
Gain in-depth knowledge of the EU Medical Device Regulation and its impact on manufacturers, notified bodies, and regulators. Equip yourself with the insights needed to guide clients through compliance challenges.
SaMD & AI
Explore the regulatory landscape for software as a medical device and artificial intelligence. Learn how to advise clients on navigating risks, innovation, and compliance in this rapidly evolving field.
Clinical & PMS
Strengthen your understanding of clinical evaluation and post-market surveillance processes. Discover how to help clients optimize these critical areas to ensure patient safety and regulatory adherence.
Global Markets
Expand your expertise in international regulatory frameworks and global reliance strategies. Support clients in achieving market access and harmonizing compliance across borders.
EU MDR Roundtable
Join focused discussions with industry leaders and regulatory experts. Share strategies and solutions to help clients navigate MDR implementation effectively.
SaMD & AI Roundtable
Collaborate with stakeholders to address the unique challenges of SaMD and AI regulation. Gain actionable insights to support your advisory services.
Clinical Evaluations & PMS Roundtable
Engage in dynamic conversations with peers and regulatory authorities to refine best practices and develop tailored solutions for clinical evaluation and PMS.







