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Table of Contents
Section 1: General Human Research Protection Program Polices 1.1 Human Research Protection Progra...
1.2 Authority Granted to the IRB and/or the Office of Regulatory Affairs (ORA) by the Organization
Last Revised: 12/17/2025 1.0 Purpose The purpose of this policy is to describe the authority gran...
2.4 IRB Review of Changes in Previously Approved Research
Last Revised 1/18/2025 For an abbreviated version intended for investigators, coordinators, and s...
1.4 UNMC Ceding Review to an External Central IRB
Last Revised: 5/15/2025 For an abbreviated version intended for investigators, coordinators, and ...
7.3 Data Registries
Last Revised: 4/16/2025 For an abbreviated version intended for investigators, coordinators, and ...
3.4 Use of Protected Health Information in Research
Last Revised: 4/9/2018 For an abbreviated version intended for investigators, coordinators, and s...
1.8 Investigational Activities Requiring IRB Review and Approval
Last Revised: 5/9/2023 For an abbreviated version intended for investigators, coordinators, and s...
Exempt Studies
It is understood this project will be conducted in full accordance with all applicable HRPP Polic...
1.5 Requirements for Research Conducted with International Sites
Last Revised: 6/10/2026 For an abbreviated version intended for investigators, coordinators, and ...
2.1 Submission for Items for Review by the IRB
Last Revised: 6/26/2026 1.0 Purpose The purpose of this policy is to describe Organization’s requ...