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IRB Policies & Guidance

IRB Policies

Introduction
Human Subjects Research Protection of Human Subjects
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
Registering Clinical Trials

Who May Serve as Principal Investigator and Mentor

Single IRB of Record Policy

 

 

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