Posts by acvazque
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 for Research has been updated to incorporate the following changes: Removal of prior requirement that only a US licensed medical doctor or a US licensed nurse practitioner may request to finalize…
Read MoreClinicalTrials.gov Registration & Report Submission
Institutional Review Board (IRB) ClinicalTrials.gov Registration & Report Submission February 6, 2026 If human subject research is subject to ClinicalTrials.gov, registration and submission of results is required. Where the protocol is investigator initiated and / or the UC Irvine Principal Investigator (PI) holds the Investigational New Drug (IND) the UC Irvine PI is responsible. A…
Read MoreResolved: ZOT IRB/hSCRO Notification Issues with Links
Visit the HRP Toolkit webpage for ZOT IRB user guides, forms, and more. Please reach out to ERA with any questions by submitting a ticket to the ERA Support Desk. The post Resolved: ZOT IRB/hSCRO Notification Issues with Links appeared first on News & Announcements.
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