As of May 23, 2022, the IRB has a new research noncompliance standard operating procedure. This new procedure can be found under Forms and Guidelines.
The new IRB software, IRBNet, is now up and running. All protocol submissions and revisions will be handled on the website. You can access the website at the following URL: IRBNet.org.
Dr. Erik Tracy, IRB Chair
The Institutional Review Board (IRB) is required by federal law to review and approve ALL research proposals that involve human subjects; that is, any research involving people including adults, children and infants. Special protections are accorded to minors, prisoners, pregnant women, and disadvantaged populations. All research conducted at UNC Pembroke or by UNC Pembroke faculty, staff and/or students at any location (including some research conducted as part of classroom exercises or course requirements) must undergo an IRB review and have a protocol application on file with the IRB Chair. Expedited reviews will be conducted on a rolling basis, and initial results from the IRB can be expected within two weeks. Applications for full-board reviews must be submitted by the 15th of the month and will be reviewed at the next full monthly IRB meeting. Protocols submitted after the 15th of the month will be considered at the following month’s meeting. For example, a protocol submitted on January 10 will be reviewed at the February meeting. A protocol submitted on January 20 will be reviewed at the March meeting. Generally, the full IRB meets on the first Wednesday of every month at 3:30PM if there are protocols that require a full board review. Additionally, the IRB accepts protocols over the summer, but researchers should expect a relatively longer time for the initial results.
There are three levels of review: Exempt from Review, Expedited Review, Full Review. The Chair determines the level of review required. Please note that an "expedited" review refers to the level of risk involved in the research not whether the researcher is under time constraints to complete the research.
Some typical examples of human subjects research the IRB reviews
- Survey research for a thesis or dissertation.
- Educational tests (cognitive, diagnostic, aptitude, or achievement)
- Research on individual or group characteristics or behavior (including research on perception, cognition, motivation, identity, language, communication, cultural beliefs, and behavior)
- Research employing survey, interview, focus group, program evaluation, human factors evaluation or quality assurance methodologies
- Collection of data made from voice, video, digital or image recordings made for research purposes
- Collection of pathological or diagnostic specimens
- Research and demonstration projects designed to study or evaluate public benefit programs
- Test and food quality evaluation studies
If you plan to undertake research in any of these areas you must submit the IRB Protocol Application, found under the Forms and Guidelines link, and any supporting materials. Along with the protocol, researchers must also submit a certificate indicating that they have completed the required CITI training courses. Researchers can register for the appropriate CITI courses at www.citiprogram.org. A PowerPoint slide detailing how to register for the CITI program and how to select the appropriate training courses can be found under “Forms and Guidelines.” The link to the CITI website can be found under “Related Links.” The IRB strongly recommends that applicants read the information under Policies and Procedures prior to the submission of the IRB Protocol Application.This website provides information about IRB policies, procedures, appeals and training opportunities.If you are not sure about whether your project requires an IRB, please contact the IRB chair.
IRB Monthly Meeting
First Wednesday of the month when needed