UPDATED NPA Routing
The workflow for the NPA has been updated. This does not impact the workflows for Non-Human Subject Research, Secondary Use, Medical Record Review, or Non-Interventional Social Behavioral and Educational Research (SBER) studies.
What is different?
- New protocols submitted after the iRIS update can proceed to IRB review even if Nursing and Pharmacy feasibility have not yet approved the submission.
- Order Sets will now be routed after Nursing, Pharmacy, and SRC approvals.
Important: While this should be uncommon, if a document is added or revised after the submission has routed to the IRB, the review has been scheduled or the submission is IRB approved, the study team is responsible for emailing the OHRS Mailbox to notify OHRS.
There are no other routing or process changes. This does not impact the subsite invite process for new protocols nor the routing to subsite feasibility reviewers.