Clinical Research Monitoring – (Certificate)

Would you like to learn (much) more about the clinical development of new innovative drug products, its ethical aspects, regulations and quality assurance? You will follow an intensive program and collaborate with other foreign students. Program aspects are history, ethics, Good Clinical Practice and quality assurance of clinical trials. During the first week of the course the theory of clinical trials will be elaborated in various lectures and the second week will be devoted to hands - on patient dossier monitoring, which belongs to the core business of a CRA, a clinical research associate. The program also includes role plays, debates and workshops, which will lead to better understanding of the ins and outs of the pharmaceutical industry in general and clinical drug development in particular.