Design and Conduct of Clinical Trials

GMS BT 575

Prereq: knowledge of biostatistics. This course covers basic principles and current methodologies used in the design and responsible conduct of clinical trials. Topics include statistical design of clinical trials, sample selection, data collection and management, patient recruitment strategies, adverse event reporting, and compliance monitoring. Practical exercises include writing clinical research protocols and informed consent forms, and designing case report forms.

FALL 2016 Schedule

Section Instructor Location Schedule Notes
A1 ARR R 5:30 pm-8:20 pm 72 E Concord St
L 203
knowledge of
MED Campus

Note that this information may change at any time. Please visit the Student Link for the most up-to-date course information.