Accelerate Regulatory Excellence: Where MedTech Leaders Share Best Practices
Guided by experts in EU MDR and IVDR to help you stay compliant and competitive
EU MDR • IVDR • Clinical & PMS • Software & AI • US & APAC • Biocompatibility • Law
The Future of MedTech Awaits: 2026 Summit Coming Soon!
The MedTech Summit 2025 may have concluded, but the journey toward regulatory excellence continues! We hope you left equipped with actionable insights, expert guidance, and valuable connections to navigate the evolving landscape of EU MDR and IVDR.
Get ready—2026 is set to be the ultimate gathering for MedTech leaders, featuring cutting-edge strategies, best practices, and unparalleled opportunities to stay compliant and competitive. Don’t miss your chance to accelerate your regulatory success. Sign up now for exclusive updates and early access to registration!
Stay in the Loop
MedTech Summit...The Numbers
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Competent Authority & Notified Body Speakers
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Leading MedTech Industry Stakeholders
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Medical Device, IVD, Software, and Combination Product Companies Represented
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Countries Represented
Top Medical Device and IVD Companies at MedTech Summit 2025
Experience the Electric Atmosphere of MedTech Summit 2025
Step into the heart of Europe’s premier medical device and IVDR conference with these captivating snapshots.
More than just images, they offer a window into the vibrant world of MedTech innovation. Experience the buzz of groundbreaking discussions, valuable networking, and the exchange of transformative ideas that shaped 2025.
Brilliant Minds, Boundless Insights – Speakers that Took the Stage in Berlin 2025!
MedTech Summit 2025 featured an unparalleled lineup of over 100 global speakers —including Competent Authorities, Notified Bodies, and top executives from companies like Abbott, Medtronic, Philips, Siemens Healthineers and Stryker.
A Snapshot of the 2025 Agenda
Discover the agenda that empowered industry leaders to drive innovation across MDR, IVDR, certification strategies, and beyond.
European Medical Device Regulations
Navigate the intricacies of the evolving European regulatory landscape and ensure you’re transition ready.
In Vitro Diagnostic Regulations
Accelerate your IVD and CDx certification journey while staying on track with EU IVDR transition goals.
Medical Device Law and Compliance
Mitigate legal risks and ensure continued compliance with the EU MDR and IVDR.
Clinical Evaluations, Investigations and Performance
Determine the right data, strengthen your claims, and streamline your clinical processes.
Software and AI for Medical Devices and IVDs
Stay ahead of the curve in the rapidly evolving SaMD and AI regulations.
Regulatory Affairs in Global Markets: US and APAC
Immerse yourself in the latest U.S. and APAC regulatory updates and gain a comprehensive understanding of global requirements.
Biocompatibility for Medical Devices
Explore the latest updates and practical applications of ISO 10993 and gain a deeper understanding of biocompatibility testing methods.
Post Market Surveillance and Vigilance
Stay aligned with current European post-market surveillance requirements and equip your team with the skills to streamline vigilance reporting.
Engage Quality Decision-Makers at MedTech Summit!
Whether you're looking to generate quality leads, showcase thought leaders, or reinforce your brand, collaborate with us to identify custom sponsorship opportunities to help you reach your business objectives.
Contact us to begin customizing your event presence today:
Kristen Schott, kschott@informaconnectls.com