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
Thank You for Attending MedTech Summit 2025
Whether you joined us virtually or experienced the buzz in Berlin, we trust MedTech Summit 2025 delivered valuable insights and connections. What's Next:
- Session Recordings: Access all presentations from Monday, 7th July, on our Streamly platform. We'll notify you by email when they're ready. *All recordings are subject to speaker permission.
- Your Feedback Matters: Watch for our post-event survey in the coming days. Your thoughts are crucial in shaping future events to meet evolving industry needs.
- RAC Holders: Ready to claim your professional credits? Visit our dedicated page for more information.
We look forward to welcoming you next year in Berlin!
Top Medical Device and IVD Companies at MedTech Summit 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.
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 inside Europe's premier medical device and IVDR conference through these captivating moments.
Were You There? Explore our full gallery and spot yourself among industry pioneers!
Missed This Year? These images offer more than a glimpse—they're your window into the vibrant ecosystem of MedTech excellence. Feel the buzz of breakthrough discussions, networking opportunities, and knowledge exchange.
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Five Days to gain the clarity, confidence, and connections to solve your problems
Lead with Compliance and Drive Innovation across MDR, IVDR, certification strategies, and everything in between.
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.
Upskill and Stay Ahead of the Curve With In-Depth Workshops
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