All correspondence, including initial studies and/or protocols progress reports, amendment requests, adverse event reports should be completed online at www.irbplus.com.
All correspondence, including initial studies and/or protocols progress reports, amendment requests, adverse event reports should be completed online at irbplus.com. If you have not submitted a study to the IRB via IRB Plus or to obtain information and access to www.irbplus.com, please click the following (click here) to complete the IRB+ Registration Form. All investigators and/or coordinators must also complete training in Human Research Protection by clicking the following link (click here). Completion of the Human Research Protection training and being given access to the electronic IRB+ submission system is required before you submit your research study.
The IRB meets at least once every month. To be included on the agenda, the submission must be entered into www.irbplus.com.
Regular office hours are 8 a.m. to 5 p.m., Monday through Friday. Please be sure to provide the Principal Investigator's (PI) name and IRB number on any correspondence relating to an existing study.
Please direct any questions to:
IRB Coordinator
405-949-4184
[email protected]
