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
+
Competent Authority & Notified Body Speakers
+
Leading MedTech Industry Stakeholders
+
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.


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
Navigating the complex regulatory landscape for MedTech can be challenging – and even more so when you’re a smaller company with less time and resources! Luckily, the MedTech Summit has designed a new interactive workshop which aims to help SMEs understand the European regulatory landscape and get their products to market. Join an esteemed array of trainers as we help you conquer everything from selecting the right vendors, to developing your regulatory and clinical strategies, to completing technical documentation, and more…
Biocompatibility Workshop: Biological Evaluation Execution and Authorship Training
Ever feel like you’ve nailed all things biocompatibility, to only then be struck down by the biological evaluation plan? You aren’t the only one! At the MedTech Summit, we understand that it can be tricky to choose the right test design for BEPs, determining relevant endpoints can be challenging, and having to manage the full lifecycle of evaluations can be a headache. Our solution? A 1-day workshop, curated by top Biocompatibility experts, to get you and your biological evaluation plans up to speed and regulatorily compliant.
EU AI Act Deep Dive Workshop
Just when you thought you’d got your head round the EU MDR and IVDR, a new regulation is introduced – welcome, the EU AI Act! Another key piece of the regulatory jigsaw, the EU AI Act adds a new level of regulation which manufacturers need to adhere to in order to get their AI-enabled devices to market – and still whilst working with limited teams and looming transition deadlines. This is why we’ve pulled together some of the best in the business to give you a hands-on look at the AI regulatory landscape, how to collect vital clinical data, and ensure lifelong compliance with robust PMS planning.
The Meeting of MedTech Minds - Competent Authorities. Notified Bodies. Industry Experts.
Get ahead of the game on the latest regulations, practical implementation and certification strategies with direct insights from the industry's biggest names
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
