Skip to main content

References

Listed below is all the known content in the system that links to this item.

1.1 Human Research Protection Program (HRPP)

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

Last Revised: 1/16/2023 1.0 Purpose The purpose of this policy is to provide a basic description ...

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...

1.17 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...

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 ...