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IRB Policies & Guidance

IRB Policies

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

Who May Serve as Principal Investigator and Mentor

Single IRB of Record Policy

 

 

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