Good Clinical Practices (GCP) in Clinical Research

GMS BT 560

This course introduces the regulatory responsibilities of sponsors, monitors, and investigators conducting clinical trials. Practical information and exercises are designed for the clinical trial professional on procedures for ensuring GCP compliance from an industry perspective. Topics include identifying and selecting qualified investigators, obtaining ethical approval to enroll patients, and initiating sites successfully. The course also covers issues related to collecting required regulatory documentation, verifying high quality data, maintaining study materials accountability, and reporting serious adverse events. Group discussions and guest speakers help students learn the practical skills used in the field.

FALL 2014 Schedule

Section Instructor Location Schedule Notes
A1 Tobia R 115 W 5:30 pm-8:30 pm 72 E Concord
R 115
MED Campus

SPRG 2015 Schedule

Section Instructor Location Schedule Notes
A1 Tobia R W 5:30 pm-8:20 pm 72 E Concord St
R 115
Mts w/GMS BT560
MED Campus

SPRG 2015 Schedule

Section Instructor Location Schedule Notes
C1 Tobia R W 5:30 pm-8:20 pm WebReg Restricted
Stamped Approval
72 E Concord St
R 115
Mts w/GMS BT560
MED Campus

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