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MedTech Summit
15 - 19 June 2026
JW Marriot, Berlin, GermanyAttend In-Person or 100% Digitally
15 - 19 June 2026
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!

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

Silvia Zancola

QARA Manager, PRRC

Theras Lifetech srl

Five days of exchanges, growth, contacts and emotions

Five days of exchanges, growth, contacts and emotions. It is one of the times of the year when you can really speak the same language and analyse together how to bring a change or even just a useful improvement to our industry.

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