Mercure Hotel MOA Berlin, Berlin, Germany,
Hybrid Event I Attend In-Person Or Digitally
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
Early Bird Savings
Save £800 when you register by midnight, Friday 6th December!
MedTech Summit 2025 Hybrid Agenda At A Glance
Take a look at the full MedTech Summit 2025 agenda at a glance to see how you and your team can benefit!
As a hybrid event, delegates will have the option to attend either in-person or digitally.
All presentations* in Berlin (*that we have permission to share from the speakers) will be recorded and made available on-demand for up to 12 months, to watch at a time that suits you.
Digital attendance - Please note only one track will be live-streamed each day and this will be indicated here shortly. Please check back soon for details.
Who Could You Be Joining At MedTech Summit
20+
Competent Authority & Notified Body Speakers
400+
Leading MedTech Industry Stakeholders
150+
Medical Device, IVD, Software and Combination Product Companies Represented
Competent Authority Guidance. Notified Body Feedback. Industry Insights.
Benchmark for best practice and get up-to-speed with the latest regulatory updates, experiences and market access expertise from our 2025 speaker line-up.
Maximise Your MedTech Summit Experience With In-Depth Training And Workshops
SME Survival Guide Workshop
Understand the EU regulatory landscape for innovation
Identify key stakeholders to bring devices and IVDs to market
Curate effective regulatory and clinical strategies
Develop and complete technical files for submission
Pinpoint funding pathways and develop pitches
Navigate pricing and reimbursement options
Biocompatibility Workshop: Biological Evaluation Execution & Authorship Training
- End to end process of biological evaluation plans
- Foundations of biological evaluations
- Test design for BEP
- Determining endpoint tests and critical factors
- Interpreting test results for analysis
- Transitioning data into BER
- Incorporating toxicology
- Lifecycle management of biological evaluation
EU AI Act Deep Dive Workshop
Comprehend the intricacies of the EU AI Act
Understand the implications for manufacturers
Identify the EU AI Act’s place in the regulatory web
Collect and demonstrate desirable clinical data
Ensure lifelong compliance with effective PMS planning
Enhance AI efficacy by exploring potential risks
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:
Neha Singh
Email: NSingh@informaconnectls.com
Put yourself centerstage
Build your personal brand. Position your company as leaders. Engage your community and peers.
Join CenterStage, Informa Connect's speaker rewards program, and get access to new opportunities to speak, create content, and get published on our online platforms. Earn points and redeem them for rewards every time you speak at an event or your content is viewed on Streamly - the new business video platform, powered by Informa, for experts, by experts like you.
You'll have member access to resources, to guide you through the process and intricacies of showcasing your stories, expertise, learnings and content across a wide range of in-person, hybrid, and virtual events.
Watch the video and click the link to find out more!