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