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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
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