Expert Insights, Tailored Networking, and Cutting-Edge Solutions Designed for Professionals Like You
MedTech Summit 2026 is the perfect event for aspiring regulatory leaders looking to advance their careers in the medtech industry. Delve into a comprehensive overview of regulatory challenges, join expert-led workshops, and learn from actionable case studies to develop your understanding and approach.
Take the opportunity to meet senior regulatory leaders from top manufacturers, hear about their career journeys, and gain insights into routes to success in the field. Explore tracks tailored to your growth, including EU MDR, SaMD & AI, and the Future Regulatory Leaders Linkup.
Young Regulatory Professionals Discount
We’re offering a 25% discount for young regulatory professionals to attend MedTech Summit and be a part of the Future Regulatory Leaders Link Up. Eligible delegates must be from a MedTech company/manufacturer, be 35 years old or under, and hold the title of Regulatory Affairs Specialist or below. Use the discount code YOUNGLEADERS at checkout to save 25% (T&Cs apply).
Tailored Programmes for Aspiring Regulatory Leaders to Develop Regulatory Mastery, Build Professional Networks, and Drive Career Success
Future Regulatory Leaders Linkup
Connect with senior leaders and peers to gain career insights, mentorship opportunities, and strategies for professional growth in the medtech regulatory field.
SME Survival Guide
Learn how small and medium-sized enterprises navigate regulatory challenges. Gain practical advice to support your career development and understanding of compliance in diverse organizational contexts.
European Regulatory Affairs
Build your knowledge of the EU Medical Device Regulation and its impact on manufacturers and regulators. Understand how MDR shapes the industry and how you can contribute to its implementation.
SaMD & AI
Explore the regulatory frameworks governing software as a medical device and artificial intelligence. Develop your expertise in this cutting-edge area to position yourself as a future leader in innovation and compliance.
Global Markets
Gain insights into international regulatory frameworks and global reliance strategies. Learn how to support manufacturers in achieving market access and harmonizing compliance across borders.
EU MDR Roundtable
Join focused discussions with industry leaders to deepen your understanding of MDR implementation and its practical challenges.
Global Markets Roundtable
Collaborate with stakeholders to explore strategies for navigating international regulatory landscapes and expanding market access.
Decode the Reforms: Real World Insights to Guide Your Next Move
Future Regulatory Leaders Link-up
Giacomo Cargnello, Head of Quality Assurance & Regulatory Affairs, C&C Solutions, Varex Imaging
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
Tackling AI Drift In Medical Devices – Impact on PMS and Beyond
Stephanie Berger, Director Global PMS, Philips