Human Research Protection Program (HRPP)
Office of the Vice President for Research
Information for IRB Members & Staff
- Determining Whether IRB Oversight is Necessary
- Determining Whether IRB Oversight is Necessary - Research on Human Specimens
- Approval of Research Involving Vulnerable Participants
- Informed Consent Process
- IRB Responsibilities for Review of Informed Consent Document and Process Through Which Informed Consent is Obtained
- Identifying Measures to Minimize Risk to Research Subject
- Finder's Fees and Bonus Payments Prohibition
- COI at Convened Meetings
- Expiration Date
- IRB Responsibility for Multi-Site Research in Which the University is Involved
- Privacy and Confidentiality
- Short Form Consent
- Reporting and Addressing Undue Influence or Coercion
- Waivers, Alterations, Substitutions, or Exceptions to Informed Consent and Patient Authorization
- Investigational Device Storage and Inventory Maintenance
- Guidance for Review and Approval of Drug and Device Studies
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