Name: 5th MedAI Regulatory & Compliance Summit
Start: 2025-03-13 00:00:00 UTC
End: 2025-03-14 00:00:00 UTC

Discover AI-driven compliance tools, global regulatory harmonization, and advanced quality control techniques to revolutionize your operations. This summit provides a unique platform to learn about practical applications from industry professionals at the forefront of these advancements.

Join us at the 5th MedAI Regulatory & Compliance Summit on March 13-14, 2025, in Munich, Germany, where industry leaders and experts will explore the latest advancements in the medical devices landscape. From leveraging cutting-edge technologies to streamline regulatory processes to optimizing compliance strategies and enhancing quality assurance, this summit delves into the transformative power of innovation in medical devices.

We are excited to introduce our esteemed speakers for the 5th MedAI Regulatory & Compliance Summit, representing leading voices in regulatory affairs, post-market clinical follow-up (PMCF), and clinical evaluation. This exceptional lineup includes:

Elizabeth Gfoeller, AT
Corporate Director, Regulatory Affairs, MED-EL GmbH
Alice Robertson, UK
PMCF Senior Executive, Purdie Pascoe
Chris Webb, UK
PMCF Manager, Purdie Pascoe
Frank Matzek, DE
VP of Regulatory & Governmental Affairs, BIOTRONIK SE & Co. KG
Leon Doorn, NL
Independent Consultant, QAIR.io
Jacqueline van Druten (MICR.CIM.RD), UK
Clinical & Regulatory Affairs Director, CLIN-R
Wiebe Postma, NL
Senior Manager Global Clinical Evaluation, BVI Medical
Fabien Roy, BE
Partner, Hogan Lovells
Annette van Raamsdonk, NL
Lead Quality and Regulatory Affairs Consultant, Emergo
Sepanta Fazaeli, NL
Clinical Systems & Medical Data Lead, Stryker
Asha Jacob, NL
Head of Regulatory Affairs & Compliance Team, Philips

Find out more at our web vonlanthenevents.com

5th MedAI Regulatory & Compliance Summit

March 13-14, 2025 | Munich, Germany

The Delegate Pass include:

In person attendance for 2 days of the conference
Access to all speakers' presentations
Networking sessions with all speakers and participants
Refreshments & coffee breaks
Lunch at the venue for both conference days
Business dinner to polish the cooperation and networking
After-event documentation package
On-line & Off-line support from our team

Key Themes & Topics

Key Practical Learning Points:

Post DOA – what did we learn and what’s still to come?
Risk management system expectations
Global perspective on combination products
PMCF surveys and their benefits
Overview of guidelines, regulations, and registration requirements
What’s the price of higher patient safety?
UDI and EUDAMED
Notified body feedback on EU MDR implementation
MDR impact on risk management and clinical evaluations
Quality management systems
Practical insights on MDR implementation from medical device manufacturers

Prerequisites & Requirements

Who should attend

Chief Executives, Vice Presidents, Directors, Heads, Leaders, and Managers specializing in:

Medical Devices • Robotics & Control • CMC (Chemistry, Manufacturing, and Controls) • Continuous Processing • Cell Culture Technology • Commercialisation • Data Integrity • Diagnostics • Quality Assurance/Control • Product Quality • Process Monitoring • Compliance • Emerging Technologies • Licensing • Lifecycle Management • Regulatory Affairs & Licensing • Risk Management • Research & Development • Track & Trace • Scale-Up & Tech Transfer • Sterilization • Supply Chain • Validation • Biotechnology • Precision Medicine • Gene Therapy • Bioinformatics • Clinical Operations • Data Science • Pharmacovigilance • Market Access • Health Economics • Artificial Intelligence Ethics

5th MedAI Regulatory & Compliance Summit

Special Offer

Location

Managed by

Vonlanthen Group s.r.o.