Content Type | Title |
---|---|
Policy | IRB Policy: Clinical Trials Guidance |
Resource | ClinicalTrials.gov |
Resource | NIH's Definition of Clinical Trial |
Resource | Federal Policy for the Protection of Human Subjects (the Common Rule) |
Resource | About the IRB Committee |
Resource | IRB Announcements & Newsletters |
Resource | IRB COVID-19 FAQs |
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 | Multi-site and Collaborative IRB Research |
Resource | Report a Concern Involving Human Participant Research |
Resource | IRB FAQs |
Resource | IRB Guidance and Resources |