IRB Review Process
Researchers are required to submit a request to the IRB for review. The request must be approved by the IRB prior to collecting data or contacting participants. The types of review conducted by IRB are:
Full Board Review & Expedited Review | Request for Review Form
Continuation Review | Request for Continued Review Form
Modification/Amendment Review | Request for Protocol Modification or Amendment Review Form
Complete the request form for the type of review necessary for research, attach the completed training certificate for all persons involved with the project, the appropriate informed consent document, and other materials involved in the study. Forward the request to the IRB Staff located in the Ottenheimer Library, room 501C. For electronic submissions, email the request to Research Compliance Officer at email@example.com. Please do not send your protocol to the IRB Chair.
For research conducted at UAMS, Arkansas Children’s Hospital Research Institute (ACHRI), or the Veterans Administration (VA), please submit the UAMS IRB Approval decision memo to the UALR IRB Staff.
If an unanticipated harmful incident or detrimental outcome is experienced by a participant as a result of participation, immediately complete the adverse event form to report the incident within 24 hours of the initial discovery. Adverse events include any incident or event that results in harm whether psychological, physical, social, legal, economic, or if it puts the participant at more than a minimal risk.
It is the responsibility of the researcher to report any incident not only in the case where there is a clear cause-effect relationship, but also when there is only a possibility that that the participant suffered harm because of their participation in the research study.