"> ');

Who Should Attend

  • 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