RELIANT Updates
January 11, 2022
Reminders to schedule a consultation with RELIANT before requesting the UW serve as the single IRB and that changes that need review for ceded studies are limited.
Non Protocol-Based Application Now Live
January 11, 2022
The non protocol-based application (nPBA) went live in ARROW on December 19th.
Updated ClinicalTrials.gov Questions Coming to ARROW
December 15, 2021
Beginning December 18, all new nPBA applications and all existing PBA applications will show new questions about registering studies with ClinicalTrials.gov.
Reminder: Single IRB Consultation Requirement
December 15, 2021
Staring January 1st, study teams will be required to have a consultation with RELIANT when asking the UW to serve as the reviewing IRB for external sites.
Review Flexibility for Single-Patient Expanded Access Requests
December 15, 2021
With the December ARROW patch, applications for HUDs and Expanded Access Requests will be stand-alone application types in the application wizard.
Non-Protocol Based Application Coming Soon
December 14, 2021
The new ARROW application designed for minimal risk research without a standalone protocol will be available soon.
VA Research Website Updates
November 17, 2021
The Madison VA templates and other tools are now being housed by the Madison VA Research Service on IRBNet.
New Single IRB Review (sIRB) Guidelines
November 17, 2021
The UW has developed new guidelines outlining when the UW will and will not serve as the reviewing IRB or cede IRB review to an external IRB.
Toolkit Updates: Short Form and Other Special Consent Processes
November 17, 2021
The Investigator Manual has been updated to describe consent guidelines for special populations that may require alternative consent processes.