Netherlands, Utrecht

Clinical Research Monitoring

when 2 July 2012 - 13 July 2012
duration 2 weeks
credits 5 ECTS
fee EUR 1095

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.

Course leader

Dr. A. A. van Dooren

Target group

Health care students (medical, pharmaceutical, nursing etc.) health care professionals who are (going to be) involved in clinical trials anyone interested in clinical trial job opportunities (CTA, CRA).

Course aim

To get thorough insight in applicable laws, rules, regulations and guidelines to the design, implementation and evaluation of clinical trials. To be able to monitor the conduction of a clinical trial and to report your findings. to communicate as a CRA (clinical research associate).

Credits info

Certificate of Attendance

Fee info

EUR 1095: Course + course materials + housing


Utrecht Summer School doesn't offer scholarships for this course.

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