Expert Insights, Tailored Networking, and Cutting-Edge Solutions Designed for Professionals Like You
MedTech Summit 2026 offers a unique platform for Notified Bodies, Regulatory Authorities, and Government representatives to connect with medtech manufacturers and regulatory leaders. Stay informed about the latest challenges facing manufacturers, from EU MDR updates to global reliance strategies, and gain insights into the evolving landscape of medical device regulations.
Participate in roundtable discussions, network with key stakeholders, and explore tracks tailored to your expertise, including SaMD & AI, Clinical & PMS, and Biocompatibility. This is your opportunity to collaborate, share knowledge, and drive innovation in the medtech regulatory space.
Tailored Programmes for Notified Bodies, Regulatory Authorities & Government Professionals to Collaborate with Industry, Exchange Expertise, and Navigate Evolving Regulatory Challenges
European Regulatory Affairs
Gain clarity on the complexities of the EU Medical Device Regulation, its implementation challenges, and its implications for manufacturers and regulators. Stay ahead of compliance requirements and ensure alignment with evolving standards.
SaMD & AI
Delve into the regulatory frameworks governing software as a medical device and artificial intelligence. Understand how innovation intersects with compliance and explore strategies to address emerging risks and opportunities.
Clinical & PMS
Strengthen your expertise in clinical evaluation and post-market surveillance. Learn how these critical processes safeguard patient safety and ensure regulatory adherence in a rapidly changing environment.
Global Markets
Expand your understanding of international regulatory frameworks and global reliance strategies. Discover pathways to streamline market access and harmonize compliance across borders.
Biocompatibility
Stay informed on the latest advancements in biocompatibility testing and compliance requirements. Ensure medical devices meet rigorous safety standards while fostering innovation.
EU MDR Roundtable
Participate in dynamic discussions with industry peers and regulatory experts. Share insights and practical solutions to address the challenges of MDR implementation.
Clinical Evaluation & PMS Roundtable
Collaborate with stakeholders to refine best practices and develop actionable strategies for clinical evaluation and post-market surveillance.
Decode the Reforms: Real World Insights to Guide Your Next Move
Streamlining EU Medical Device Conformity Assessment: Navigating the proposed Annex VII Implementing Act
Goran Adburrahman, Senior IVD Product Specialist, TÜV Rheinland
Giacomo Cargnello, Head of Quality Assurance & Regulatory Affairs, C&C Solutions, Varex Imaging
Marta Carnielli, Head of Certification IVD, TÜV SÜD
James Shearn, Director, Regulatory Intelligence & Policy, Steris
Keynote Panel: EU MDR Revisions – The Headlines, Implications and What’s Ahead
Jeppe Larsen, Director of Medical Devices, Danish Medicines Agency
Andreas Stange, Senior Vice President, MHS Regulatory & Quality, TÜV SÜD
Erik Vollebregt, Partner, Axon Lawyers
Nataliya Deych, Vice President Regulatory Affairs EMEA, Latam, Canada Edwards Lifesciences
Bassil Akra, CEO, AKRA TEAM