Informed Consent Essentials

This course is essential for Investigators, study coordinators and anyone involved in consenting participants in research projects. In this foundational course, we will cover the following topics:

What is informed consent?

Why is it important?

Overview of regulations and campus policies/procedures that apply

Who can give consent?

Tailoring the consent process to the target population

Participant understanding of the study

Documenting consent

Note: As of May 2025, plans are underway to develop a complimentary course specific to informed consent in clinical trials.  Details will be announced soon. Please contact [email protected] if you would like further information.