Chestnut's Institutional Review Board (IRB) reviews, approves, and conducts periodic review of research involving human participants. Chestnut's IRB is required by federal regulations to review all research projects involving human participants in which (a) the conduct or recruitment of research participants involves Chestnut staff or patients; (b) the research is conducted by or under the direction of any Chestnut employee in connection with his/her institutional duties; (c) the research involves the use of Chestnut's patient information. Prior to the initiation of any research, it must first be reviewed and approved by Chestnut's IRB.
In accordance with federal regulations, Chestnut’s IRB is composed of individuals with expertise, experience, and diversity in academic, research, and professional backgrounds. The IRB meets once per quarter.
In order for a project to be considered by the IRB, the following forms must be completed:
Survey and data collection instruments, related forms, and when applicable, an informed consent, should be submitted with the completed IRB forms.
For questions about Chestnut's IRB or to submit your completed IRB forms, please send an email message to Kelli Wright, Research Services Coordinator, at email@example.com