JW Marriot, Berlin, Germany,
Attend In-Person or 100% Digitally
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
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.
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
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.
Top Medical Device and IVD Companies at MedTech Summit 2025
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.
Explore the 2025 Workshops: Actionable Solutions for MedTech Leaders
SME Survival Guide Workshop
Navigating MedTech regulations can be challenging, especially for SMEs with limited resources. The MedTech Summit’s new interactive workshop helps you understand the European regulatory landscape, guiding you through vendor selection, regulatory strategies, clinical planning, and technical documentation. Join expert trainers and get your product to market faster!
Biocompatibility Workshop: Biological Evaluation Execution and Authorship Training
Struggling with biological evaluation plans? You're not alone! Join our expert-led, one-day workshop at the MedTech Summit to master test design for BEPs, manage full lifecycle evaluations, and get both you and your biological evaluation plans up to speed and regulatory compliant—without the headache.
EU AI Act Deep Dive Workshop
The EU AI Act has arrived, adding another layer of regulation for AI-enabled devices. With looming transition deadlines and limited resources, compliance can feel overwhelming. Join top experts at the MedTech Summit for a hands-on workshop to navigate the regulations, gather essential clinical data, and ensure long-term compliance with robust PMS planning.
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