Session Datesort descending
The History of Human Subjects Research and Foundations for Regulations 03/19/2025 - 2:00pm EDT to 05/02/2025 - 3:00pm EDT
Determining What Qualifies as Non-Human Subjects Research. 04/16/2025 - 10:30am EDT to 05/16/2025 - 11:30am EDT
Understanding the Regulatory Differences Between Exempt, Expedited, and Greater than Minimal Risk Research. 05/21/2025 - 2:00pm EDT to 06/21/2025 - 3:00pm EDT
Single IRB-Internal and External IRBs; Use of Commercial IRBs (CIRB, Advarra, WCG) 06/18/2025 - 10:30am to 11:30am EDT
Ethics Training, CITI, and Discussing the Nature of Ethics Requirements vs. moral judgments in protection human research participants 07/16/2025 - 2:00pm to 3:00pm EDT
Conducting Participant-Centered Informed Consent Processes 08/20/2025 - 10:30am to 11:30am EDT
Documenting Consent Forms and Procedures; Documenting Research Enrollment—Utilizing Systems Adequately (IRBNet; Florence; On-Core) 09/17/2025 - 2:00pm to 3:00pm EDT
The Basics of Getting Started to Submit a Research Project to the IRB, Ancillary Review Types, and Less Common Submissions 10/15/2025 - 10:30am to 11:30am EDT
Post IRB Approval Monitoring and Auditing of Research - Is It Just the IRB?—Auditing Requirements (Electronic, In-Person) 11/19/2025 - 2:00pm to 3:00pm EST
Non-Regulatory Reviews in Your IRB Submission —Why is the IRB Asking for this Information? Review Institutional and State Policies 12/17/2025 - 10:30am to 11:30am EST