Office of Research Integriy

The Medical IRB reviews all biomedical research involving human subjects (including VAMC and FDA-regulated research). IRB members include individuals with a broad range of expertise. The Medical IRB members are appointed by the Director of the Office of Research Integrity.

All research involving the use of human subjects subject to the Marshall University Human Research Protection Program MUST be submitted to an IRB designated by Marshall University for review and approval PRIOR to initiation of the project.

Investigators

Initial Protocol Application Package

Protocol Flow Chart

Meeting Dates/Deadlines

Huntington VA Medical Center
Protocol Submission Forms

Conflict of Interest Checklist (Word PDF)

Expedited Categories 1-9

AE/SAE/Problem Report Form

Consent Templates/Waivers

Continuing Review Instructions

Continuing Review Protocol
Assessment Checklist

Modification Protocol
Assessment Checklist

Emergency Use Letter Template

Members

IRB#1 Member List

Meeting Dates

Forms for Members

Education Requirements

Conflict of Interest Checklist (Word PDF)

IRB Guest Non-Disclosure

Ethics Reports

The Belmont Report

Declaration of Helsinki

Nuremberg Code
(Directives for Human Experimentation)

Standard Operating Procedures

Marshall University HRPP SOP Manual

Regulations

HIPAA

Code of Federal Regulations

(45 CFR 46)

Links

VHA Handbook 1200.5

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