| Policy #1 |
Determining Whether a Research Activity Needs IRB Review or Exemption From IRB Review |
| Policy #2 |
Submission Requirements and Procedures for Requests for 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 |
Recruitment and Payment of Human Participants |
| SOP 10 |
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 |
| SOP 14 |
International Human Research |
| SOP 15 |
Informed Consent, Enrollment, and Other Considerations for
Research Involving Cornell Students |
| SOP 16 |
Computer- and Internet-Based Human Participant Survey Research |
| SOP 17 |
Protocol Principal Investigator's Roles and Responsibilities |
| SOP 18 |
New York State Laws Relevant to Human Participation Research |
| Policy #19 |
Use of Physiological Devices, Biomedical Procedures or Biological Samples in Research |
| Policy #20 |
Use of Social Networking Sites and Mobile Devices for Human Participant Research |
| Policy #21 |
Triennial (Three Year) Approval For Research Studies |
