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Table of Contents

HRPP Policies and Procedures

Section 1: General Human Research Protection Program Polices 1.1 Human Research Protection Progra...

5.1 Obtaining Informed Consent From Research Subjects

HRPP Policies and Procedures Section 5: Informed Consent

Last Revised: 1/8/2025 For an abbreviated version intended for investigators, coordinators, and s...

6.2 Research Involving Investigational and Marketed Devices

HRPP Policies and Procedures Section 6: FDA Regulated Research/Drugs...

Last Revised: 1/23/2024 For an abbreviated version intended for investigators, coordinators, and ...

6.1 Research Involving Investigational and Marketed Drugs

HRPP Policies and Procedures Section 6: FDA Regulated Research/Drugs...

Last Revised: 1/24/2024 For an abbreviated version intended for investigators, coordinators, and ...

1.27 Research Personnel Qualifications and Responsibilities

HRPP Policies and Procedures Section 1: General Human Research Prote...

Last Revised: 11/26/2025 For an abbreviated version intended for investigators, coordinators, and...

1.3 UNMC IRB Serving as the Single IRB for Multisite Research

HRPP Policies and Procedures Section 1: General Human Research Prote...

Last Revised: 4/21/2025 For an abbreviated version intended for investigators, coordinators, and ...

1.1 Human Research Protection Program (HRPP)

HRPP Policies and Procedures Section 1: General Human Research Prote...

Last Revised: 2/18/2026 1.0 Purpose The purpose of this policy is to provide a basic description ...

1.17 Retention of Research Records

HRPP Policies and Procedures Section 1: General Human Research Prote...

Last Revised: 12/17/2025 For an abbreviated version intended for investigators, coordinators, and...