IRB-101 Virtual Training Sessions


Are you new to the IRB submissions process and in need of some guidance? Please attend one of our IRB 101 Training Sessions!


IRB 101: IRB staff will cover basic types of submissions including initial applications, continuing reviews, modifications, and reportable events. We’ll also provide an overview of how to use the Human Subjects Research Application (HS-ERA) system to submit applications to the IRB for review.


Informed Consent 101: IRB staff will cover definitions of informed consent, types of consent, required elements of consent, waivers of consent, and more.


Sessions will last 90 minutes to allow time for Q&A. Sessions will be held via Zoom.

Any questions can be directed to Diana Floegel, Senior Regulatory Analyst, at


Sign up for the sessions below here:

  • Thursday, November 2, 1-2:30pm: Social Behavioral IRB 101
  • Thursday, November 9, 1-2:30pm: Biomedical IRB 101
  • Thursday, November 16, 1-2:30pm: Informed Consent 101
  • Thursday, November 30, 1-2:30pm: Biomedical IRB 101