Aims of the program
The EU Regulatory Affairs course aims to provide a certification in the area of EU Drug/Medical Device 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 (extract; subject to change)
- DI Dr. Salma Michor, MBA, RAC, Michor Consulting e.U
- Dr. Siegfried Schmitt, Parexel Consulting
- Dr. Wirthumer-Hoche