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1.29 ClinicalTrials.gov Reporting

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

Last Revised: 3/20/2023 1.0. Purpose The purpose of this policy is to describe the requirements ...

2.2 Full IRB Review

HRPP Policies and Procedures Section 2: Process of Review

Last Revised: 10/13/2022 1.0 Purpose The purpose of this policy is to describe the Organization’s...

2.3 Expedited Review

HRPP Policies and Procedures Section 2: Process of Review

Last Revised 1/24/2024 1.0 Purpose The purpose of this policy is to describe the Organization’s r...

2.4 IRB Review of Changes in Previously Approved Research

HRPP Policies and Procedures Section 2: Process of Review

Last Revised 1/18/2025 1.0 Purpose The purpose of this policy is to describe the Organization’s r...

2.7 Continuing Review of Research

HRPP Policies and Procedures Section 2: Process of Review

Last Revised 1/12/2024 1.0 Purpose The purpose of this policy is to describe the Organization’s r...

5.1 Obtaining Informed Consent From Research Subjects

HRPP Policies and Procedures Section 5: Informed Consent

Last Revised: 1/8/2025 1.0 Purpose The purpose of this policy is to describe the Organization’s r...

8.2 Review of Study Related Complaints

HRPP Policies and Procedures Section 8: AEs, Unanticipated Problems ...

Last Revised: 5/8/2023 1.0 Purpose The purpose of this policy is to describe the process for repo...

8.3 Review of Unanticipated Problems Involving Risk to the Subject or Others

HRPP Policies and Procedures Section 8: AEs, Unanticipated Problems ...

Last Revised: 5/8/2023 1.0 Purpose The purpose of this policy is to describe the process for repo...

8.7 Reporting Incidents to Institutional Officials and Federal Agencies

HRPP Policies and Procedures Section 8: AEs, Unanticipated Problems ...

Last Revised: 8/1/2023 1.0 Purpose The purpose of this policy is to describe the Organization’s r...