11th EDITION EUROPEAN MEDICAL DEVICE AND DIAGNOSTICS CLINICAL EVIDENCE STRATEGY CONFERENCE
Belgium | 2027
A Dual Track Conference
Regulatory Confidence & Innovation Advantage – Driving Inspection Readiness, Practical Execution and the Future Clinical Strategy
key information
- Brussels, Belgium
- 23rd – 25th February 2027
#EUCES2027
Conference Insight
Step into three days of innovation, collaboration, and strategic thinking, bringing together Europe’s leading professionals in Clinical Evidence, Regulatory Affairs, Medical Affairs, IIS, PMCF, Clinical Investigations, and Digital Transformation.
Gain practical insights, exchange ideas with industry leaders, and discover forward-thinking strategies to navigate today’s challenges and shape tomorrow’s medical device landscape.
- Dual Conference Tracks
- Interactive Workshops
- Industry-Led Panel Discussions
- Engaging Roundtable Discussions
- High-Value Networking
3 DAYS OF INSIGHTS & INNOVATION
Two Dedicated Tracks - Today’s regulatory challenges | Future-focused clinical strategies
PRE-CONFERENCE WORKSHOP DAY
- PMCF Strategy & Execution
- MDR/IVDR Clinical Evidence Compliance
- AI & Digital Technologies for Clinical Evidence
- Real-World Data (RWD) & Real-World Evidence (RWE)
- Clinical Data Ecosystems & Evidence Strategy
CONFERENCE DAY 1 & 2
- MDR/IVDR Updates & Notified Body Expectations
- Global Clinical Evidence Strategies
- Investigator-Initiated Studies (IIS)
- NOTIFIED BODY PANEL: Clinical Evidence Under Review: Insights, Expectations & Common Deficiencies
- ROUNDTABLE DISCUSSION: Operational Challenges in Clinical Evidence & PMCF
CONFERENCE DAY 1 & 2
- AI-Enabled Clinical Evidence Generation
- Cybersecurity & Connected Medical Devices
- Digital Transformation & Future Operating Models
- PANEL DISCUSSION: Will AI Fundamentally Reshape Clinical Affairs?
- ROUNDTABLE DISCUSSION: Future Clinical Innovation & Digital Transformation
Our Industry Specialists
Dr Alexander Reiprich
Carine Cochereau
Daniel Carter
Dr Arne Böhling
Kirsten Welz
Ate Loonstra
Dr Marcin Maj
Andriani Daskalaki
Chrystelle Coudert-Koall
Richard Holborow
Nebojsa Serafimovic
Marta Carnielli
Nunung Nur Rahmah
Dr Sharmila Gardner
Marianna Mastroroberto
Dr Marco Marchetti
Benedicte Nuyttens
Filippo Bagni
Paola Vivoda
Dr Gaston Westergaard
Why Take Part
The 11th Edition European Medical Device & Diagnostics Clinical Evidence Strategy Conference brings together Europe’s leading medical device professionals to exchange knowledge, share best practices, and explore emerging approaches shaping the future of the industry; an invaluable opportunity to gain practical insights, benchmark strategies, overcome shared challenges, and connect with the experts driving innovation and progress.
Network & Benchmark
Engage with 100+ industry professionals to share experiences, discuss challenges, and explore practical solutions across clinical strategy, trials, and compliance
Stay Ahead of Regulatory Expectations
Understand the latest MDR/IVDR developments, notified body expectations, and compliance strategies to strengthen readiness and support effective decision-making
Deep-Dive Sessions
Participate in detailed sessions on Clinical Evidence, AI & Digital Transformation, RWE, CER, PMCF & PMS, and ethical issues in healthcare innovations
Practical Takeaways
Move beyond theory with implementation-focused case studies, proven approaches, and actionable solutions you can apply within your organisation.
KEY TAKEAWAYS
Building a Lifecycle Clinical Evidence Strategy
Develop an integrated evidence roadmap that aligns clinical evaluation, PMCF, real-world evidence, and post-market activities to support compliance and long-term product success.
From CER to Continuous Evidence (Case Study)
Learn practical approaches to designing and executing PMCF programmes that generate robust data, satisfy regulators, and create clinical value.
Real-World Evidence: From Data Collection to Regulatory Acceptance
Understand how to identify, collect, and leverage real-world data to strengthen clinical evidence and support regulatory submissions across global markets.
Bridging Clinical, Regulatory, and Medical Affairs
Discover strategies to improve cross-functional collaboration, ensuring evidence generation aligns with regulatory requirements, clinical objectives, and business priorities.
Inspection Readiness and Evidence Defensibility
Strengthen documentation, traceability, and evidence governance to improve preparedness for audits, notified body reviews, and regulatory inspections.
Futureproofing Your Clinical Evidence Strategy
Prepare for evolving MDR expectations, global regulatory changes, and emerging evidence requirements by building scalable, data-driven clinical evidence programmes.
Moments Captured
Take a glimpse into the highlights of our conferences, where ideas come to life and connections are made
Our Testimonials
An insightful conference with valuable discussions on clinical strategy and PMCF, supported by useful real-world examples from the industry.
– Clinical Evaluation Manager
The conference was very well organised with relevant topics. It was helpful that the format allowed direct communication between industry and Notified Bodies. The conference format included various ways of communication facilitation.
– Senior Clinical Evaluations Manager
Inspiring and motivating to connect with peers and be reminded of the bigger picture.
– Clinical Development Scientist
A true value-add and great opportunity to gain real insight from other manufacturers.
– Global Clinical Affairs Manager
Super organised, well-thought-out agenda. Speakers were passionate and dedicated Experts.
– Lead Scientific Manager
The conference provided useful insights across several areas. I found the sessions on Clinical Strategy, RWE to PMCF, Global Clinical Compliance, and AI Tech particularly helpful and came away with new ideas to consider in my work.
– Scientific Manager
A fantastic learning experience that combined expert guidance, real-world examples, and genuine connection with colleagues across the MedTech community.
– Clinical Affairs Specialist
A great conference with high-quality discussions on MDR clinical evidence requirements and valuable networking opportunities.
– Clinical Evaluations Manager
Interesting topics, well-performed event, engaging discussions and lessons learned!
– Senior CRA
Good event, plenty of networking opportunities. Good environment to share knowledge, challenges, approaches and perspectives with those in similar roles!
– Clinical Research Manager
Very well-organised conference where experience and knowledge are shared in a friendly and collaborative environment.
– Senior Clinical Affairs Manager
Lovely networking experience full of knowledge.
– Scientific Manager
YOUR ALL-IN-ONE GUIDE TO THE EVENT
Get the full scoop on what’s in store!
Explore the event overview and dive into the agenda for the 11th Edition European Medical Device and Diagnostics Clinical Evidence Strategy Conference — your gateway to 3 days of strategy, science, and innovation.
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