September 12, 2017: If your study is industry sponsored, please upload a completed HREBA Billing Information Form to the “REB Service(s) Fee” section in IRISS. Click title above to access the form.
August 11, 2017: A new Reportable Event Guidance has been adopted by the Clinical Trials Committee. Please follow this new guidance when submitting SAEs, Safety Update Reports, Protocol Deviations, Audits, Privacy Breaches, Participant Complaints, and DSMB/Interim Analysis Reports. Note that files within IRISS are to use the Reportable Events feature for these submissions.
June 28, 2017: A new Reportable Event feature is available in IRISS. This feature is available for studies reviewed by the HREBA-Cancer Committee and HREBA-Clinical Trials Committee. If your study was reviewed by the Community Health Committee, please continue submitting Reportable Events (e.g. SAEs, protocol deviations, DSMB reports, etc.) as per the existing process.
HREBA’s Three Committees
The three committees of HREBA work together as one board. For a full list of all HREBA members, please click here.
The Institutional Research Information Services Solution
HREBA’s three committees manage all ethics submissions and reviews through the IRISS on-line platform.
If you are already familiar with the committee that you need to submit your ethics applications through, start by registering on IRISS. Once you have registered you may submit your ethics application online. If you have questions, contact email@example.com
Scheduled maintenance: Sundays from 1:00 am to 3:00 am
Please ensure you are logged off the system during this time
as work that has not been saved will be lost.