Home /  Courses And Programs / CT: Human Subjects Protection and IRBs

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.

Other Credits: BRN: 16 CE hours.

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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