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