Institutional Review Board

The Institutional Review Board (IRB) Office serves as the central hub for 麻豆传媒映画 University鈥檚 Enterprise Human Research Protection Program (HRPP). The 麻豆传媒映画 IRB is fully accredited by the Association for the Accreditation of Human Research Protection Programs (AAHRPP), reflecting the University鈥檚 commitment to the highest standards of ethical and regulatory oversight in human subjects research. Guided by the ethical principles of the Belmont Report and applicable federal, state, and institutional regulations, the IRB oversees human subjects research to minimize risk, ensure informed consent, and protect research participants.

The IRB is authorized to approve, exempt, modify, monitor, or disapprove research involving human subjects. IRB approval or an official determination of exemption is required before any study-related activities may begin.

The IRB Office supports the research community by providing education, consultation, and submission guidance, fostering a culture of integrity, accountability, and respect for research participants across the University.

Mission

The mission of the 麻豆传媒映画 Institutional Review Board (IRB) is to safeguard the rights, dignity, and well-being of individuals who participate in research. Through high-quality review, education, and guidance, we promote ethical, compliant, and responsible human subjects research across the University.

Contact Us

Research Institutional Review Board

irb@augusta.edu

706-721-3110

Contact Us

Research Compliance

Health Sciences Campus
麻豆传媒映画, GA 30912

706-721-1483

800-576-6623

(Institutional Compliance Hotline)

Emergencies: For after-hours research subject-related emergencies, please call the IRB Office at 706-721-3110.

Resources for Investigators

Tools for Researchers Database

Access the Tools for Researchers database to view IRB-related and institutional policies. Enter a search term鈥攕uch as IRB, IRB templates, IRB policy, IRB guidance, Exempt, or Expedited鈥攖o review a list of relevant documents matching your search.

Tools for Researchers

Online Human Subjects Determination (OHSD) Form

The Online Human Subjects Determination (OHSD) form is an electronic tool that collects key project details to determine if an activity qualifies as human subjects research and whether IRB review is required. Effective November 1, 2025, this will be the sole method for HSDs.

IRB Study Consultation

Study-specific guidance for investigators developing or preparing to submit a research protocol. Focuses on IRB requirements, review category, and submission planning for a defined project.

IRB Training Session

General education on IRB processes, policies, and regulatory basics. Designed for investigators and research staff seeking foundational or refresher training.

IRB Virtual Walk-In Wednesday: Webinar Series

A recurring webinar series covering the full research protocol lifecycle鈥攆rom study planning and IRB submission through post-approval requirements and close-out. Designed to provide practical guidance and promote consistent, ethical research practices.

Protocol Builder

Protocol Builder is an online tool that helps investigators create IRB-ready human subject research protocols with all required elements for scientific and ethical review.

IRB Training Videos

Our IRB Training Video Archive contains a wide range of videos designed to educate human subjects researchers on ethical principles, regulatory requirements, and the IRB submission process.

Getting Started Guide for IRB Submissions

The Getting Started Handbook is a helpful resource for investigators, providing a detailed overview of the required tasks and documents for various types of study submissions, including new studies, amendments, and reportable events.

CITI Program Training

All investigators are required to complete the appropriate CITI Program training courses prior to engaging in human subject research activities at AU.

IRB Office Internship

The 麻豆传媒映画 IRB Office Internship provides Master of Public Health students with practical, hands-on experience in human subjects protections, research ethics, and IRB operations. This 2-credit hour internship requires a minimum of 75 field hours over one semester.