EU Regulatory Affairs

Certified Program
Master of Science in EU Regulatory Affairs

Aims of the program

The EU Regulatory Affairs course aims to provide a certification in the area of EU Drug/Medical Device Regulatory Affairs. Students can proceed to complete a Masters degree in EU Regulatory affairs.

**) The tuition fees do not include the costs of the RAC certification and any extra courses offered by RAPS as preparation for the exam. Candidates taking the RAC/EU exam offered by RAPS will have to register separately via the RAPS website:


Lecturers in alphabetic order

  • DI Dr. Salma Michor, MBA, RAC, Michor Consulting e.U
  • Dr. Siegfried Schmidt, Parexel Consulting
  • Dr. Wirthumer-Hoche, AGES (BMGF)
  • Dr. Gudenus, Granzer Regulatory Consulting & Services
  • DI Martin Schmid, encotec Schmid KEG

Stipendien & Förderungen


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