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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
Book Early and Save!
Save £600 when you book by midnight, Friday 17th January
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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
MedTech Summit 2025 Hybrid Agenda at a Glance
Take a look at the 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 speaker-approved sessions will be posted On Demand post-event 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.
Meet the Competent Authority, Notified Body and Industry Packed Speaker Line-up
Become the expert on the latest regulations, practical implementation and certification strategies with direct insights from the industry's biggest names
Upskill at MedTech Summit with In-Depth Workshops and Training
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 and 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
