Content Type | Title |
---|---|
Resource | About the IRB Committee |
Resource | The Life Cycle of an IRB Protocol |
Resource | IRB Announcements & Newsletters |
Process | Research with Human Participants |
Resource | Submit or Manage Your IRB Protocol |
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 | IRB Considerations for Clinical Trials |
Resource | Multi-site and Collaborative IRB Research |
Resource | Report a Concern Involving Human Participant Research |
Resource | IRB FAQs |