Content Type | Title |
---|---|
News | IRB News: New Training Requirement for Exempt Research |
Training | CITI Online Courses for Cornell Researchers (COI, IRB, RCR, Export Control) |
Resource | IRB CITI Course Completion Records |
Resource | CITI Program |
Resource | NIH Policy on Good Clinical Practice Training |
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 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 |
Resource | IRB Guidance and Resources |