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References

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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...

2.6 Exempt Research

HRPP Policies and Procedures Section 2: Process of Review

Last Revised: 1/7/2024 For an abbreviated version intended for investigators, coordinators, and s...

6.5 Expanded Access to Investigational Drugs and Devices for Treatment Use

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

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

6.3 Humanitarian Use Device (HUD)

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

Last Revised: 5/26/2021 For an abbreviated version intended for investigators, coordinators, and ...

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...

6.1 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 ...

5.2 Waiver or Alteration of Informed Consent and HIPAA Authorization

HRPP Policies and Procedures Section 5: Informed Consent

Last Revised: 2/7/2024 For an abbreviated version intended for investigators, coordinators, and s...

Emergency Treatment

Institutional Review Board (IRB) Guidebook Procedures

The contact list for Emergency Treatment authorization can be found here in RSS. Under certain ci...