Full Board and Expedited research must be submitted through the Human Subject Research (HSR) Portal prior to submitting to COMIRB. Research protocols which are exempt do not need to be submitted through the HSR Portal. When you receive a clearance letter from the HSR Portal, attach that to your COMIRB submission.
Contact Health Data Compass for research access to and use of data sets from UCHealth Epic.
If you would like COMIRB to serve as the Single IRB for a multicenter study, contact COMIRB@ucdenver.edu.
On October 1, 2020, COMIRB assumed IRB oversight for human subjects research at UCHealth formerly under the oversight of the UCHealth IRB. COMIRB is working in close collaboration with UCHealth Research Administration, such that we do not require investigators to take any other specific action with COMIRB until you otherwise need IRB review (e.g., submitting and amendment, continuing review, or unanticipated problem).
For more information is available here:
|Cardiology, Surgery, Trauma|
Ryan Lowry, IRB Manager, Panels A&B
Mary Glennon, IRB Specialist, Panels A&B
|Nursing & Pharmacy||Cat Sutherland, Assistant Directorfirstname.lastname@example.org|
Melissa Smith, IRB Manager, Panels D&S
|Other||Mary Glennon, IRB Specialist, Panels A&Bemail@example.com|
|System Director, Research Administration||Laurie Blumberg-Romero, MA, CRAfirstname.lastname@example.org|
|IRB Liaison||Kim Bueningemail@example.com|
|Director, Research Administration –Southern Colorado||Elizabeth Graffirstname.lastname@example.org|
|Director of Research Administration – Northern Colorado||Sara Twomblyemail@example.com|
|Chief Privacy Officer||Erika Riethmillerfirstname.lastname@example.org|