Human Subjects
All research at Georgia State University (GSU) that involves human subjects must be reviewed and approved in accordance with federal law and GSU policy. GSU's Institutional Review Board (IRB) is charged with overseeing compliance with these federal regulations. The goal of these regulations is to ensure the safety, respect, and dignity of human subjects who volunteer to participate in scientific research, and to provide public accountability for the trust which the public places in institutions conducting such research.
Electronic Submission of IRB Applications
All applications to the IRB will be made through IRBWise . This system enables faculty , students and staff to submit an application electronically.
It also allows for on-line monitoring of protocols, submitting adverse events, renewals and amendments.
Required Education and Training
All researchers, staff, students, and others who interact with human subjects in the performance of research and assisting in research must complete required on-line educational program on the Collaborative IRB Training Initiative (CITI), a comprehensive web-based program before the Institutional Review Board (IRB) may accept a proposal.
Informed Consent Process
All subjects must be adequately consented to participate in research. A model informed consent form is provided to assist the researcher with this endeavor. If minors are to be a part of the research activity proper assent and parental permission must be obtained.
The IRB meets once monthly. Those protocols that require that require review by the full board must be submitted by the posted deadline .
A complete list of the IRB members and their area of expertise is provided.
The list serve was created to distribute updates and other relevant changes through email to all Principal Investigators.
The IRB Manual contains the rationale, responsibilities, policies, and regulations for the IRB.
Additional Information
IRB Staff
For questions you may contact:
Susan Vogtner, BBA
Compliance Specialist
Phone: (404) 413-3513
Shelia White, PhD, CIP
Compliance Officer
Phone: (404) 413-3514






