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Contacting the HRP
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Frequently Requested InformationÂ
IRB Biomedical Member Roster
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General Information Often Requested by Study Sponsors
HRP Fast Facts
CARE-Q Certified
UCI IRB FWA# 00004071
A Federalwide Assurance (FWA) is an assurance of compliance with 45 CFR part 46 submitted to the Office for Human Research Protections (OHRP).
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UCI IRB IORG# 0000236
Institutional Review Boards (IRB) are operated by IRB organizations (IORG). The IORG number is a unique number assigned by OHRP.
Revised Continuing Review Submission Process for Single IRB
An archived version of this message may be found at news.research.uci.edu Human Research Protections Revised Continuing Review Submission Process for Single IRB Which studies are impacted? ...
Read More SAVE THE DATE: Topic-Specific QRAM (07/15)
Dear Colleagues: Please mark your calendars for an off-cycle Quarterly Research Administration Meeting (QRAM) on Wednesday, July 15, 2026 from 2:00-3:00PM. Sponsored Projects will be hosting ...
Read More Consent Templates & the Witness Signature Box
An archived version of this message may be found at news.research.uci.edu Human Research Protections (HRP) Institutional Review Board Consent Templates & the Witness Signature Box Effective ...
Read More ZOT IRB / hSCRO System Update — Enhancements & Bug Fixes
Dear IRB Staff and Researchers, We are pleased to announce that ZOT IRB and hSCRO will be updated with the latest enhancements and bug fixes on ...
Read More Food and Drug Administration (FDA) Guidance on Safety Reporting
An archived version of this message may be found at news.research.uci.edu Human Research Protections (HRP) Institutional Review Board Food and Drug Administration (FDA) Guidance on Safety ...
Read More Changes to the Consent Process and Biomedical Consent Template
Effective March 1, 2026: HRP has made changes to the consent process and biomedical consent template. Please note the following: HRP-090 SOP – Informed Consent Process ...
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