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
