Medical Devices - Regulatory Affairs - programme structure

Semester 1

  • Introduction to regulatory affairs
  • Development and risk management
  • Practical project - regulatory requirements
  • Clinical evaluation and academic writing
  • Quality and process management
  • Practical project - quality management and clinical validation

Semester 2

  • Area of specialisation regulatory affairs
  • Focus module 1
  • Focus module 2
  • Project work

Semester 3

Master's thesis

Degree awarded

Master of Science in Medical Devices - Regulatory Affairs