IRB Main > IRB Policy & Standard Operating Procedures
IRB - Human Participants Policy & Standard Operating Procedures
Policies
- Charge - Cornell University Institutional Review Board for Human Participants
- Decision Tree - Is your activity covered under the Human Research Protection Program?
Procedures
| Policy Number |
Policy Name |
| SOP 1 |
Determining Whether a Research Activity Needs IRB Review or Exemption From IRB Review |
| SOP 2 |
Requirements for Submission of Research Protocols for a Determination by ORIA of Exemption from IRB Review |
| SOP 3 |
Initial and Continuing Review by the IRB: Requirements for Submission of Applications, Approval Criteria, and Expedited and Convened Committee Review Procedures |
| SOP 4 |
Unanticipated Problems Involving Risk to Human Research Participants or Others: Procedures for Reporting to, and Review By, the IRB |
| SOP 5 |
Managing Noncompliance in Human Research Protection Program |
| SOP 6 |
Suspensions and Terminations of IRB Approval of Research Protocols |
| SOP 7 |
Reporting Unanticipated Problems, Noncompliance, Suspensions, and Terminations to Regulatory Agencies and Sponsors |
| SOP 8 |
Closure of a Research Protocol |
| SOP 9 |
Informed Consent Options, Processes, and Documentation |
| SOP 11 |
Informed Consent, Enrollment, and Other Considerations for Research Involving Children |
| SOP 12 |
Informed Consent, Enrollment, and Other Considerations for Research Involving Prisoners |
| SOP 13 |
Informed Consent, Enrollment, and Other Considerations for Research Involving Normal, Healthy Participants |
