CLRA 520 Clinical Study Administration I

Provides an overview of the development, content and planning process of the clinical research study. Topics include roles and responsibilities, ICH GCPs, clinical research ethics, clinical study protocol, informed consent, and institutional review boards (IRBs).

Credit 3 hrs May not be repeated for additional credit
Grade Mode Normal (A-F) Course Rotation Fall (in-person)

Prerequisites - CLRA 510 may be taken concurrently
Restriction by Major -
Restriction by Degree Type - Graduate standing

Additional Information - Students who can not satisfy enrollment restrictions may request department permission to enroll; enrollment is not guaranteed.

Equivalent Course(s) -
Course History -
Change to description, prerequisites, and corequisite 2/2024, effective Fall 2024; Course Rotation added 9/2014, Course Revision 7/2014, Updated 2/2013, effective Summer 2013; May 2011

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