IRB Policies
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| Introduction |
| Human Subjects Research Protection of Human Subjects |
| Registering Clinical Trials |
| Off-Hours Coverage of Research Participants |
| IRB Membership |
| Initial Review of Research Projects |
| Continuing Review of IRB-Approved Research Projects |
| Review of Amendments in Previously Approved Projects |
| Suspension or Termination of IRB Approval |
| Investigations of Unauthorized or Noncompliant Research |
| IRB Record Keeping |
| Submission of Reports of Adverse Events |
| Research Involving Minors as Participants |
| Research Involving Pregnant Women as Participants |
| Subject Recruitment Advertisement and Incentives |
| Cooperative Research |
| IRB Confidentiality Policy and Procedures |
| IRB Review of Research to be Performed Off Site |
| Certification of Study Team Members |
| Policy 5026 Research Misconduct.pdf |
| Review of Grant Proposals by IRB |
| Substituted-Surrogate Consent |
| Obtaining Informed Consent from Human Subjects |
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Who May Serve as Principal Investigator and Mentor
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Single IRB of Record Policy
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