Congress Topics

Topics to be covered in RAMD 2018

  • The Role of the European Authorized Representative in the New MDR / IVDR Era
  • Optimizing Generation of Clinical Evidence for Medical Devices
  • Post Market Surveillance: from Reducing Risks to Value Creation
  • Medical Devices Cybersecurity and a Data Transfer Management, What we Need to Know
  • Health Economics: Getting Ready for Health Technology Assessment
  • The Impact and Consequences of the New EU MDR / IVDR
  • The Regulatory Process for Medical Devices in China
  • Medical Devices - New Rules & Guidance for Indian Market
  • The New European Regulation (MDR) from a Notified Body Perspective
  • What to Consider When Developing a Clinical Strategy for CE Marking of a New Medical Device
  • Human Factors and Design for Usability of Medical Devices