Find guidance on funding and agency updates during the federal government transition (updated 10/23/2025)
| Content Type | Title |
|---|---|
| Policy | IRB Guidance: Clinical Trials |
| Resource | ClinicalTrials.gov |
| Resource | NIH's Definition of Clinical Trial |
| Resource | Federal Policy for the Protection of Human Subjects (the Common Rule) |
| Process | Research with Human Participants |
| Resource | About the IRB Committee |
| Resource | The Life Cycle of an IRB Protocol |
| Resource | IRB Announcements & Newsletters |
| Resource | IRB Informed Consent |
| Resource | IRB Training |
| Resource | IRB Considerations: Human Participant Data, Data Sets and Internet Research |
| Resource | IRB Biomedical Research |
| Resource | IRB Considerations for International Research |
| Resource | Multi-site and Collaborative IRB Research |
| Resource | Report a Concern Involving Human Participant Research |
| Resource | IRB FAQs |
| Resource | IRB Guidance and Resources |