2nd Annual European MedTech Summit Berlin
BERLIN | 2025
International in-person conference filled with leading industry speakers.
key information
- Location: NH Berlin Alexanderplatz, Landsberger Allee 26, 10249 Berlin, Germany
- Part of the PPM World Tour
- June 11-12, 2025
- 9:00 - 17:30 Local Time
What to expect
The European MedTech Summit is a gathering of the sharpest minds in medical devices, all under one roof. We’re bringing together two worlds of expertise into one unforgettable event. That’s exactly what you’ll find at our combined Project & Portfolio Management and Medical Device Safety & Compliance Conference in Berlin.
For two packed days, you’ll be immersed in the latest trends, challenges, and game-changing ideas. Over 40 industry experts will share their insights, real-world experiences, and inspiring visions. Whether you’re deep into strategy or focused on the nitty-gritty of regulations, there’s something for everyone.
It’s not just about listening; it’s about connecting. Network with like-minded professionals, share your experiences, and together, let’s shape the future of medical devices. Come to Berlin and be part of a community that’s passionate about making a difference.
Track 1
Medical Device Project & Portfolio Management
Unlock the pursuit of excellence in project management with insights from industry leaders. Learn about strategic planning, stakeholder relationships mastery, agile methodologies, and effective data management in the ever-evolving pharmaceutical landscape across all domains, including R&D, clinical development, manufacturing, quality assurance, supply chain, and business development.
- Digital Transformation and Integration of AI
- Supply Chain Disruptions
- Accelerating Time-to-Market without Compromising Quality
- Innovating Under Pressure: Managing Risk and Speed in MedTech Projects
- Agile PPM for Medical Devices
- Optimizing Resource Allocation
- Talent Management and Development in Medical Device
- Navigating Global Regulatory Affairs
Track 2
Medical Device Safety & Compliance
World’s greatest minds in drug safety, pharmacovigilance, data analysis, reporting, government policy, and innovative technology united under the Why Summits will delve into cybersecurity, regulatory challenges, patient safety and human factors engineering. You can expect networking with like-minded professionals and learn the latest trends, challenges, and game-changing ideas.
- Regulatory Hurdles and Ethical Considerations of AI in Medical Devices
- Proactive Cybersecurity
- EU MDR/IVDR Compliance Challenges
- Building Strong Quality Management System
- Effective Medical Device Vigilance Process
- Post Market Surveillance & RWD
- Balancing Safety and Sustainability: The Next Frontier in Medical Device Design
- Patient-Centric Device Development and Usability
Target audience breakdown:
-
- Medical Device Safety
- Risk Management
- Signal Detection
- Regulatory & Quality
- Post-market Research
- VPs, Global Heads and Senior Directors of:
- Digitization
- Automation
- Operations
- Program & Portfolio Management
- Project Management
-
- Supply chain
- Cybersecurity
- RWE & RWD
- Resource Management
- Vigilance
Medtech
M – Meet the brightest minds in the industry
E – Explore cutting-edge solutions
D – Discover trends shaping the future
T – Transform challenges into opportunities
E – Engage in meaningful connections
C – Collaborate to drive innovation
H – Harness the power of shared expertise
Elevate Your PV Game:
Mastering the 5 W’s
Who, What, When, Where, and Why are the cornerstones of effective process management and continuous improvement. Asking the right questions leads to meaningful answers—enabling you to set up processes with precision and drive greater effectiveness.
At our summit, dive into HOW to turn these foundational elements into actionable strategies that deliver measurable results. Learn. Innovate. Lead.
Everything you need to know about this event in one spot.
Check out our event overview and agenda and discover 2nd Annual European MedTech Summit Berlin.
Event Speakers
Yasmin Mahua
Senior Regulatory Affairs Specialist
J&J MedTech
Jens Melander
Managing Director
Patch & Sparks Inc
Cédric Kahl
Global Senior Project Leader & Portfolio Manager for the Clinical Diagnostic Group
Former Bio-Rad Laboratories
Verena Kieferle
Director Global Regulatory Affairs
Vantive
Lorenz Strehl
Market Expansion Lead UK/IR
Flinn.ai
Carsten Mahrenholz
Founder and CEO
COLDPLASMATECH GmbH
Baoleri Lee Rauhe
Regulatory Specialist, Global Regulatory Affairs
Radiometer Medical Aps.
Maria Han
Regulatory Specialist, Global Regulatory Affairs
Radiometer Medical Aps.
Andrew Whytock
Head of Digitalization, Pharma Business Segment
Siemens
Ariana Adjani
Co-Founder and MD
FINE TREATMENT
Peter Fairhurst
Director Programs and Projects
NovoNordisk
Fatima Sanfourche
Sr. Director of QA & RA Compliance for Medical devices, Combination products and eHealth
Bayer
Mircea Ciuca
Global Head Medical Safety
Organon
Edwige Strippe
Director Global Regulatory Affairs, Medical Device Group
Santen
Pavel Kušnierik
Head of Regulatory Affairs
Contipro
Andreas Silber
Director of Global Pricing
Dentsply Sirona
Marta Carnielli
Head of Certification IVD
TUV SUD GmbH
Renea Schønemann Olsen
Senior Post-Market Surveillance Manager, Scientific Affairs
3shape
Massimo Kubon
Vice Dean of Faculty Engineering & Technology: Marketing & International Affairs
Furtwangen University
Marta Martínez
Senior Vigilance Process Manager
Novartis
Maurizio Zaccheddu
Senior Quality Assurance Manager
Medela
Leo Hovestadt
Director Government Affairs EU
Elekta
Benjamin Rochette
Vice President, Global Regulatory Affairs
Coloplast
Tim Rumbaugh
Vice President Program Management
Edwards Lifesciences
Event Partners
GOLD PARTNER
The team at Flinn.ai specializes in developing software solutions that automate quality and regulatory compliance processes for medical device and pharmaceutical manufacturers. Their solution enables medical device manufacturers to automate post-market surveillance tasks, such as monitoring safety databases, reviewing literature, and handling customer complaint data. This ensures comprehensive compliance and significantly reduces manual effort.
GOLD PARTNER
Patch & Sparks delivers exceptional value to their clients by offering two leading tools—Planisware and OnePlan — for Strategic Portfolio Management, as well as Project and Portfolio management. Each platform excels in distinct areas, and their expertise ensures that they can recommend and implement the solution that best fits each client’s unique needs.
Testimonials
