Would you like to know 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 monitoring aspects 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 clinical research associates (CRAs).
Period
08-07-2013 - 19-07-2013 (2 weeks)
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.
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)
Credits
5.0 ECTS credits
Certificate of Attendance
Course fee
EUR 1380: Course + course materials + housing + mealplan
EUR 895: Course + course materials + lunch
Course leader
Dr A. A. van Dooren
Scholarships
Utrecht Summer School doesn't offer scholarships for this course.
Utrecht University
Address: PO BOX 80148
Postal code: 3508 TC
City: Utrecht
Country: Netherlands
Website: http://www.utrechtsummerschool.nl
E-mail: summerschool@uu.nl
Phone: 0031302534400
Clinical Research Monitoring
label
Diverse
calendar_month
2013-01-07, 00:00
autorenew
2025-09-29, 17:00
history_edu
Silviu Marinescu
