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Navigating the Path to Quality and Regulatory Excellence in the Medical Device Sector

European Medical Device Summit 2025
  • Addressing the impact of MDR on the medical device industry
  • Sharing insights on developing and implementing effective Quality Management Systems (QMS)
  • Exploring the delicate balance between innovation and safety requirements
  • Discussing strategies to conduct quality risk assessments and act proactively
  • Setting a path forward for the medical device industry with best practices and lessons learned
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Steve Blatcher
Product Development Director
Team Consulting
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Kamaal Anas
CVP, Regulatory Affairs, B. Braun Medical
B. Braun Group
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Romain Denis
VP, Global Regulatory and Quality Affairs
Intuitive Surgical
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Carine Cochereau, Ph.D.
VP, Regulatory International
Integra LifeSciences
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Michael Schiffner
VP, Quality and Technology
Siemens Healthineers