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.
Read MoreZot IRB/HSCRO Downtime – Saturday, January 17, 2026 11:30AM thru 9:30PM PST.
Dear Colleagues, Huron will be performing scheduled maintenance tomorrow, Saturday, January 17th from 11:30AM thru 9:30PM PST. Zot IRB/HSCRO will be down during this period. Please be sure to save your work and exit out of the system prior to the downtime. Please let the ERA Team know if you have any questions – you…
Read MoreZOT IRB/hSCRO Notifications: Issues with Links
Dear UCI Huron Community, We are experiencing an issue with the hyperlinks embedded in Zot IRB/HSCRO email notifications that is causing some users to be taken to the Dashboard instead of the study submission or workspace referenced in the email. ERA and OIT are actively working towards a resolution. There are a few workarounds to…
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