Who Should Attend & Why?

WHO SHOULD ATTEND RMD2025?

  • European Professionals / Responsible Persons
  • Medical Device Companies
  • Clinical Professionals
  • Safety Assessors/QA Personnel
  • Project Managers
  • Notified Bodies
  • Regulatory Affairs Specialists
  • R&D Personnel
  • Professionals in the field of Medical Devices and IVD
  • CEOs
  • CROs / CRAs
  • Research Facility Managers
  • Pharmaceutical Company Representatives
  • Start-up Companies

 

WHY ATTEND RMD2025?

  • Stay Updated
  • Knowledge Sharing and Learning
  • Exposure to New Technologies
  • Regulatory and Compliance Updates
  • Market Intelligence and Trends
  • Professional Development
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