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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 study teams - please visit here: sIRB 1.0 Purpose The purpose of this policy is to describe the Organization’s requirements for the UNMC IRB to serve as the Single...

audience
faculty

1.4 UNMC Ceding Review to an External Central IRB

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

Last Revised: 5/15/2025 For an abbreviated version intended for investigators, coordinators, and study teams - please visit here: cIRB 1.0 Purpose The purpose of this policy is to describe the Organization’s requirements for the UNMC IRB to cede review to an e...

1.5 Requirements for Research Conducted with International Sites

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

Last Revised: 5/9/2023 For an abbreviated version intended for investigators, coordinators, and study teams - please visit here: International Research 1.0 Purpose The purpose of this policy is to describe the Organization’s requirements for research conducted...

1.6 IRB Composition, Leadership, Qualifications, and Responsibilities

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

Last Revised: 2/15/2025 1.0 Purpose The purpose of this policy and procedure is to describe the Organization’s requirements for IRB composition, leadership, member qualifications, and responsibilities. 2.0 Policy It the policy of the Organization that the mem...

1.7 IRB Member, Consultant, Staff and Guest Conflict of Interest Identification and Management

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

Last Revised: 9/25/2024 1.0 Purpose The purpose of this policy is to describe the Organization’s requirements for the identification and management of IRB member, consultant, staff and guest potential conflicts of interest. For the purpose of this policy, sta...

1.8 Investigational Activities Requiring IRB Review and Approval

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

Last Revised: 5/9/2023 For an abbreviated version intended for investigators, coordinators, and study teams - please visit here: What Requires IRB Review and Approval 1.0 Purpose The purpose of this policy is to describe the investigational activities that req...

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 requirements for resources that are necessary for human subject protection, care of research participants, and safety during the conduct of research. 2.0 Policy I...

1.10 Scientific and Other Committee Review of Research

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

Last Revised: 4/8/2025 1.0 Purpose The purpose of this policy is to describe the Organization’s requirements for scientific and scholarly merit review, and for review by other component committees of the HRPP, of all non-exempt human subject research conducted...

1.11 HRPP Access to Legal Counsel

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

Last Revised: 2/11/2025 1.0 Purpose The purpose of this policy is to describe the Organization’s requirements for HRPP access to legal counsel for the purpose of interpreting federal, state, and local law. 2.0 Policy It is the policy of the Organization that ...

1.12 Sponsored Research

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

Revised: 6/12/2024 1.0 Purpose The purpose of this policy is to describe the Organization’s requirements for research sponsored by an external funding agency or commercial sponsor for which the UNMC IRB is the IRB of record. Organization and Sponsor requireme...

1.13 Compliance with ICH-GCP Guidelines

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

Last Revised: 10/17/2025 1.0. Purpose The purpose of this policy is to describe the Organization’s requirements for compliance with the International Conference on Harmonization (ICH) Good Clinical Practice (GCP) E6 Guidelines. 2.0. Policy It is the policy of...

1.14 Research Subject to Department of Defense Regulatory Requirements

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

Last Revised: 1/10/2024 1.0 Purpose The purpose of this policy and procedure is to specify the Organization’s requirements for the review, approval, conduct and oversight of human subject research funded by or involving the U.S. Department of Defense (DoD) and...

1.15 Research Subject to Department of Justice Regulatory Requirements

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

Last Revised: 11/12/2025 1.0 Purpose The purpose of this policy is to specify the Organizations requirements for the review, approval, conduct and oversight of human subject research funded by or involving the U.S. Department of Justice (DoJ) and the Federal B...

1.16 ORA Record Keeping Requirements

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

Last Revised: 01/17/2024 1.0 Purpose The purpose of this policy is to describe the Organization’s requirements for maintenance of documentation of IRB and ORA activities. Retention of records by the investigator is described in HRPP policy 1.17 (Retention of R...

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 study teams - please visit here: Retention of Research Records 1.0 Purpose The purpose of this policy is to describe the requirements for retention of research re...

1.18 Review and Approval of HRPP Policies

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

Last Revised: 11/13/2024 1.0 Purpose The purpose of this policy is to describe the Organization’s requirements for the review and approval of HRPP policies. 2.0 Policy It is the policy of the Organization to continually assess the adequacy of existent policie...

1.19 IRB Signature Authority

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

Last Revised: 10/7/2022 1.0 Purpose The purpose of this policy is to describe the Organization’s requirements for granting signature authority for Office of Regulatory Affairs (ORA) and IRB correspondence. 2.0 Policy It is the Organization’s policy that the I...

1.20 Community Involvement in Outreach Activities and Community Based Participatory Research (CBPR)

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

Last Revised: 1/17/2024 1.0 Purpose The purpose of this policy is to describe the Organization’s outreach activities to enhance the public’s understanding of research, obtain feedback about any community concerns, disseminate results of research conducted by t...

1.21 Post-Approval Monitoring of Research

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

Last Revised: 11/17/2025 For an abbreviated version intended for investigators, coordinators, and study teams - please visit here: Post-Approval Monitoring of Research 1.0. Purpose The purpose of this policy is to describe the Organization’s requirements for p...

1.22 Assessment of the Effectiveness and Efficiency of the HRPP

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

Last Revised: 9/25/2024 1.0 Purpose The purpose of this policy is to describe the Organization’s requirements for assessment of the quality, effectiveness, efficiency and support of the Organization’s HRPP in carrying out its mission to ensure protection of hu...