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MedTech Summit

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16 - 20 June 2025
Mercure Hotel MOA Berlin, Berlin, GermanyHybrid Event I Attend In-Person or Digitally
16 - 20 June 2025
Mercure Hotel MOA Berlin, Berlin, Germany,
Hybrid Event I Attend In-Person or Digitally

Where the MedTech Regulatory Industry Meets

The Leading Medical Device and IVD Regulatory Affairs Event in Europe

Master the End-To-End Certification Pathway. Streamline Global Market Access. Maintain Compliance. With Expert Guidance from Competent Authorities, Notified Bodies and Industry

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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

Hybrid by Design – Experience MedTech Summit Your Way!

Explore the MedTech Summit agenda at a glance and discover how you and your team can benefit!

Whether you choose to attend in person or digitally, the hybrid format ensures you don’t miss out on any of the cutting-edge insights, live sessions, and exclusive networking opportunities.

Click here to see what’s included in the digital pass.

From Brussels to Berlin!

Whether you joined us in Brussels or missed out, check out the highlights from MedTech Summit 2024 for a glimpse of what’s in store in Berlin! Join us to experience Europe’s leading event for Medical Device and IVD Regulatory Affairs.

Don’t get left behind - with all the top companies attending, the only thing missing is you!

Upskill and Stay Ahead of the Curve With In-Depth Workshops

SME Survival Guide Workshop

This workshop will give you the expertise to navigate EU regulations, engage with key stakeholders, develop effective regulatory and clinical strategies, complete technical files for submission, secure funding, perfect your pitch, and understand pricing and reimbursement.

Biocompatibility Workshop: Biological Evaluation Execution and Authorship Training

Join the Biocompatibility Workshop and master the end-to-end process of biological evaluations. Learn how to design tests for BEP, interpret results for analysis, determine endpoint tests and critical factors, incorporate toxicology, and manage the full lifecycle of evaluations.

EU AI Act Deep Dive Workshop

Dive deep into the EU AI Act and understand its intricacies and impact on manufacturers. Learn to navigate AI in the regulatory landscape, collect and demonstrate vital clinical data, and ensure lifelong compliance with robust PMS planning. Explore key risks and enhance the efficacy of your AI solutions.

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.

Connect With Key Decision Makers at MedTech Summit 2025

Whether you're increasing your company profile, launching a new product or creating business development opportunities, we have a package to suit your needs.

We can provide flexible and tailored solutions to optimise your investment.

For information on how your organisation could benefit from this hybrid event and to discuss the full range of lead generating, networking and branding opportunities, please contact

Kristen Schott at kristen.schott@informa.com