Clinical Research Monitoring
HU University of Applied Sciences Utrecht
Healthcare (HU)
Healthcare (HU)
Course code: M25
Advanced bachelor level
Advanced bachelor level

LOCATION
COURSE DIRECTOR
Dr A. A. van Dooren
LECTURERS
Dr A. A. van Dooren and Prof. Dr G. Fortwengel, Hannover (FRG)
TARGET GROUP
Health care students (medical, pharmaceutical, nursing etc.) health care professionals who are (going to be) involved in clinical studies. Anyone interested in clinical trial job opportunities (CTA, CRA).
Minimum number of attendants: 10, maximum 25.
Minimum number of attendants: 10, maximum 25.
COURSE AIM
To get a thorough insight in applicable laws, rules, regulations and guidelines for the design, implementation and evaluation of clinical trials.
to get an understanding of the ethical considerations influencing clinical drug trials To be able to monitor the conduction of a clinical trial and to report the findings.
to communicate as a CRA (clinical research associate)
to get an understanding of the ethical considerations influencing clinical drug trials To be able to monitor the conduction of a clinical trial and to report the findings.
to communicate as a CRA (clinical research associate)
PERIOD
08 July 2013 - 19 July 2013 (2 weeks)
CREDITS
5.0 ECTS credits + Certificate of Attendance
STUDY LOAD
6 hours a day + self study
FEE
• € 1380 - Course + course materials + housing + mealplan
• € 895 - Course + course materials + lunch
• € 895 - Course + course materials + lunch
Students from universities that have a MOU with the Faculty of Healthcare of HU Utrecht University of Applied Sciences may be entitled to a fee reduction. To be arranged with the course director before application.
DISCOUNTS AND COMBINATIONS
» Overview of all available discounts
SCHOLARSHIPS
Utrecht Summer School doesn't offer scholarships for this course.
MORE INFORMATION
REGISTRATION
Deadline for registration: 17 June 2013
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