Why do you need to provide informed consent to clinical research subjects? What are the Principal Investigator’s responsibilities for a clinical research study? What are successful strategies in working with the Institutional Review Board (IRB)? Our regulatory courses provide information on how clinical research studies need to ensure participant safety and welfare while complying with federal, state, and institutional regulations.

Clinical Trial Billing Compliance

Does your clinical trial qualify for insurance coverage?

Instructor: Douglas Reichgott Course Type: Self-Paced Online
A Team-based Approach to Data and Safety Monitoring Boards

What is a Data Safety and Monitoring Board (DSMB), and how can it improve your study?

Instructor: Tamsin Knox, Farzad Noubary, Julie SantaCroce Burt Course Type: Self-Paced Online