Search Results

After the funded project is complete, UNMC must administratively close out the project with the sponsor and internally. Technical Reporting In general, a final technical report should include: Summary of progress made toward the achievement of the origina...

2025 Ethical Study Design IS Good Science (Susan Fish) The AI Middle Game: From Panic to Proportionate IRB Oversight (Tonya Ferraro) Integrating IRB Review Into US Special Pathogens Research Efforts (Kristi DeHaai & Abby Lowe) Informed Consent: Why We ...

In line with most other academic medical centers and universities, the Office of Regulatory Affairs and the IRB charges an initial submission and an annual continuing review fee for commercial and industry sponsored protocols. New Pricing Guidelines (effective...

TRANSFERS IN AND OUT Traditionally sponsors make awards to institutions/organizations and not to an individual therefore special processes are in place to allow for the transfer of a grant whether an investigator is joining UNMC or leaving UNMC. TRANSFERS TO...

Study teams are responsible for reporting noncompliance to the IRB/ORA. This page serves as a guide for study teams when deciding what constitutes noncompliance, when it needs to be reported, and how to report it. The following Noncompliance Guide will explain...

NIH requires the use of Common Forms for Biosketch and Other Support documents for applications due on or after January 25, 2026. The Common Forms will also be required for RPPRs, JITs, and prior approval requests submitted on or after January 25, 2026. Senio...

To support studies impacted by an outage, investigators should use the following temporary downtime procedures. If your study uses the impacted service to collect data related to subject safety or to deliver surveys, questionnaires or other data collection ma...

As a condition for NIH funding, all research subject to the NIH Guidelines for Research Involving Recombinant or Synthetic Nucleic Acid Molecules (NIH Guidelines) must be reviewed by the UNMC Institutional Biosafety Committee. Examples of clinical trials subj...

Advertisement Policy Cheat Sheet Central IRB (cIRB) Cheat Sheet Coded vs De-Identified Data Compensation Cheat Sheet Consent for Non-English Speaking Subjects Cheat Sheet Direct Invitation Policy Cheat Sheet Reimbursement Cheat Sheet Short Form Cheat Sheet Sin...

E-Signature Instructions RSS Guides

Assembling your Research Team IRB Acronyms and Definitions Informed Consent Resources Other Institutional Requirements

IRB Application Guide

Information regarding IRB Board meetings and Submission deadlines can be found on the IRB & Submission Deadlines page.