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References

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1.9 Resources Necessary to Protect Subjects

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

Last Revised: 1/16/2025 1.0 Purpose The purpose of this policy is to describe the Organization’s ...

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...

2.7 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...

2.9 Closure of On-Going Research

HRPP Policies and Procedures Section 2: Process of Review

Last Revised: 08/10/2023 1.0 Purpose The purpose of this policy is to describe the criteria for, ...

3.2 Data and Safety Monitoring

HRPP Policies and Procedures Section 3: Special Issues

Last Revised 12/22/2022 1.0 Purpose The purpose of this policy is to describe the Organization’s ...

8.1 Review of Adverse Events and Adverse Device Effects

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

Last Revised: 5/4/2023 1.0 Purpose The purpose of this policy is to describe the process for repo...

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...

8.4 Review of Noncompliance Involving the PI or Study Personnel

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

Last Revised: 3/6/2024 1.0 Purpose The purpose of this policy is to describe the process for revi...

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...