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Complete Review Assessment After accessing a review request from your system inbox, the review management page will display for the application you've selected. Read the instructions provided in the gray text box for specific review requirements for the comp...

From time to time, you may be asked to serve on a review committee for an internal competition. When the application is ready for review in the NURamp system, you will receive an email indicating that applications are ready for your review. Log in to the NUR...

Last Revised: 1/23/2024 For an abbreviated version intended for investigators, coordinators, and study teams - please visit here: Expanded Access to Investigational Drugs and Devices 1.0 Purpose 1.1. The purpose of this policy and procedure is to describe the...

Federated Access Users from University of Nebraska institutions may log in to the UNMC Research Support Services application to schedule core services and view billing statements. Click the appropriate logo for your institution of the Research Support Servic...

Navigate to nuramp.nebraska.edu. Using your institutional credentials, sign in to the system. You will need to use Duo two-factor authentication to sign in. In the top right corner of your screen, click the "add" button, then select "Add New Application" ...

Last Revised: 12/17/2025 For an abbreviated version intended for investigators, coordinators, and study teams - please visit here: Obtaining Informed Consent for Non-English Speaking Persons Obtaining Informed Consent for Persons with Additional Needs 1.0 Purp...

Last Revised: 8/31/2023 1.0 Purpose The purpose of this policy is to describe the Emergency Preparedness and Continuity of Operations Plan (EP/COOP) for the HRPP. This policy and accompanying documents focus on the Office of Regulatory Affairs (ORA) and the I...

Last Revised: 9/1/2023 1.0 Emergency Preparedness /Continuity of Operations Plan (EP/COOP) 1.1. Purpose The UNMC Office of Regulatory Affairs (ORA) and the Human Research Protection Program (HRPP) is committed to the safety and protection of research partic...

SPAdmin is under the direction of the Vice Chancellor for Research and is organized as follows: Director Beth DeCarolis Assistant Directors Kris Morrissey (Contracts Team) Laura Wise (Grants Team) Grants/Contracts Specialists & Office Associates (see below) St...

Mailing Address: Institutional Review Board University of Nebraska Medical Center 987830 Nebraska Medical Center Omaha, NE 68198-7830 Phone: 402-559-6463 Email: irbora@unmc.edu The Institutional Review Board (IRB) is a committee formally const...

It is understood this project will be conducted in full accordance with all applicable HRPP Policies. It is also understood that the Office of Regulatory Affairs (ORA) will be immediately notified of any proposed changes for a research project that: Affect t...

Check back to this page for more updates regarding clinicaltrials.gov information. Please contact oract.gov@unmc.edu for more information. When submitting a request for a new user account for ClinicalTrials.gov, please provide the following information to or...

New Biomedical/Social Behavioral IRB Application Rollout Oct 30th, 2025 The new version of the Biomedical/Social Behavioral IRB application will be active in RSS on November 10th, 2025. All Biomedical/Social Behavioral applications on the current form must bes...

The IRB has multiple tools to assist investigators in determining whether their project is Human Subject Research and requires IRB review: This link will provide a guide on what Human Subject Research is as opposed to what is not: Am I Doing Human Subject Re...

IRBs IRB-01 (Adult) OHRP IRB Registration # IRB00000670 Meets the first Thursday of each month (excluding January and July) IRB-02 (Adult) OHRP IRB Registration # IRB00000671 Meets the third Thursday of each month IRB-03 (Rapid Response) OHRP IRB Re...

There are eight applications to choose from depending on the type of research that is planned. Please make sure that you select the correct application type for your research. Once started, responses from one application cannot be transferred directly to a dif...

The purpose of this policy is to provide a basic description of UNMC’s Human Research Protection Program (HRPP) through: 1) the Organization’s stated mission, 2) application of ethical principles to guide all human subject research under the oversight of the O...

Report a problem Report a problem securely and confidentially through the UNMC Human Subjects Research Comment Portal. Are you a research subject, staff or investigator who wants to report a complaint or problem to the IRB? By following the comment portal link...