IRB: Human Research Participants Protection

IRB policies related to the review of research activities are listed below. For a full list of IRB policies and procedures, including administrative policies, please navigate to the IRB folder within the RRP.

IRB: Human Research Participants Protection
Alteration or Waiver of Informed Consent for Research Subjects
Continuing Review of Approved, Ongoing Studies (RA-IRB-111)
Determining Whether an Activity is Research Involving Human Subjects (RA-IRB-118)
Elements and Documentation of Informed Consent for Research Subjects (RA-IRB-200)
Emergency and Expanded Use of a Test Article (RA-IRB-211)
Enrollment of Subjects Who Do Not Read, Speak, or Understand Written or Spoken English (RA-IRB-202)
Expedited Initial Review of Research (RA-IRB-105)
International Research (RA-IRB-122)
Lapse of IRB Approval for Ongoing Studies (RA-IRB-112)
Managing Research Prior to Departure Sabbatical Medical Leave or Other Absence (RA-IRB-214)
Modification or Amendment of IRB Approved Research (RA-IRB-110)
Process of Obtaining Additional Expertise for IRB Review (RA-IRB-107)
Protocol Exceptions and Deviations (RA-IRB-210)
Reporting and Review of Unanticipated Problems, Including Adverse Events (RA-IRB-209)
Research Involving Adults with Questionable Capacity to Consent (RA-IRB-208)
Research Involving Children (Minors) (RA-IRB-206)
Research Involving Investigational Devices (RA-IRB-114)
Research Involving Investigational Drugs (RA-IRB-115)
Research Involving Neonates of Uncertain Viability or Non-Viability (RA-IRB-204)
Research Involving Pregnant Women or Fetuses (RA-IRB-203)
Research Involving Stem Cells and Fetal Material, including Dead Fetuses and Placenta (RA-IRB-205)
Review and Approval of Study Advertisements and Other Recruitment Methods (RA-IRB-116)
Review of Humanitarian Use Device (RA-IRB-212)
Review of Research Activity that May Meet the Regulatory Criteria for Exempt Status (RA-IRB-104)
Review of Research by Auxillary Committees (RA-IRB-119)
Review of Research by IRBs outside of Rush University Medical Center (RA-IRB-120)
Review of Research by the Full IRB (RA-IRB-106)
Review of Research Materials by IRB Administrative Staff (RA-IRB-113)
Suspensions and Terminations of Approved Research (RA-IRB-213)