Institutional Review Board
Columbus State University promotes and supports human research. Basic tenets of human research are voluntary participation and the ethical treatment of the subjects in the research process. The basic ethical principles are defined in the Belmont Report. The Code of Federal Regulations (CFR) defines the basic rules by which research should be evaluated (45 CFR 46). The purpose of the IRB is to ensure that the rights and welfare of all human subjects are protected.
How to complete and submit an application:
- Carefully read all CSU IRB Policies and Procedures. Failure to follow policies and procedures may lead to significant delays in the processing of your application.
- Complete the Human Research Application. (If you are a student or you are not affiliated with CSU, then you must list a CSU faculty member as the Co-PI.)
- Create the Addendum composed of all supporting materials. All supporting materials should be a merged into one PDF or Word file separate from the Application.
- Human subject research training certificates for every member of the research team. If you need to complete the training, the NIH Office offers a free training course.
- Copies of all recruitment materials (print and electronic).
- Obtain a Letter of Cooperation from each off-campus site if applicable.
- Copies of all research measures, protocols, and instruments.
- Complete the Informed Consent template if applicable. For internet surveys and other web-based projects, complete the Web-based Informed Consent template. For additional IC templates see the Additional Forms section below.
- Complete the Application Checklist to verify all necessary elements are completed/included. It is not necessary to submit this checklist to the IRB.
- Email the completed application as an attachment and the addendum as a second attachment to email@example.com from the researcher's CSU email account. Students must copy (cc) their supervising faculty member on all correspondence with the IRB.
Visit the FAQ page for additional information related to completing an application and addendum, modifying approved research, and concluding approved research.
- Lab Personnel Form- All lab/department personnel human subjects research training certificates must be included in a separate merged addendum.
- Alternate Informed Consent Templates
Making Changes to Ongoing Research:
- Project Modification Form- If supporting materials are required for the modification request, all documents should be merged into one Addendum document and submitted with the modification form as a separate attachment.
End of Research (Expedited and Full):
- Final Report Form - To be used if data collection for the study is completed.
- Project Continuation Form - To be used if you plan to continue collecting data for the study. If changes need to be made to the protocol as well, you must submit a project modification form and supporting addendum along with the project continuation form.
Average Processing Times (as of 9/01/16)
- Exempt Protocols are 5 days.
- Expedited Protocols are 14 days.
Please note that processing times will be slower during the summer, and that the IRB is closed during all CSU holidays or breaks.