This essential course offers an ethical framework for human subjects regulations, introduces regulatory issues in clinical trials, and reviews concern for human subjects protection in drug/device trials. A mock IRB meeting applies the principles learned.
Note: Required course in Professional Certificate program. Prerequisite: FPM 40173, The Drug Development Process.
Course Number: FPM-40388
Credit: 2.00 unit(s)
Related Certificate Programs: Clinical Trials Design and Management
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4/27/2020 - 5/31/2020
7/6/2020 - 8/9/2020