Institutional Review Board
Additional resources regarding the Institutional Review Board.
|Consent form guides & templates||Application & submission guides||IRB members|
|human subjects research training||security of data||irb meetings|
|what is human subjects research?||external resources||frequently asked questions|
|10/01/2020||Step-by-step guides for completing your IRB submission can be found on the IRB GeauxGrants help desk webpage.|
|08/12/2020||Policy on Return to Human Subject Research|
|08/01/2020||If you need to amend your study and your study was approved prior to July 1, 2020, you will need to complete the Transitional Amendment in GeauxGrants.|
|07/01/2020||IRB applications must now be submitted through GeauxGrants.|
|06/01/2020||Graduate and undergraduate students are no longer allowed to act as Principal Investigators (PIs) on projects that require IRB approval. If a student submits the application, the supervising professor will need to be listed as the PI.|
The primary goal of the Institutional Review Board (IRB) is to ensure the safety, health, and privacy of human subjects in research and scholarly projects.
The IRB is responsible for ensuring compliance with the federal requirements that govern all research with human subjects (funded or not), unless projects meet specific criteria for exemption.
The IRB aims to assist faculty in the conduct of successful studies with human subjects, by helping them meet the criteria for IRB approval.
As of July 1, 2020, all projects must be submitted via GeauxGrants for approval or exemption. In no event may a project with human subjects begin before IRB exemption or approval is received.
Non-exempt projects must be reviewed and approved at a convened meeting of the IRB, except for certain minimal risk projects that qualify for an expedited review performed by one or more IRB board members. Projects must then be re-reviewed by the IRB no more than 365 days after approval (at a full IRB meeting if the original approval required full IRB review), even if the start date of the research is postponed. The IRB office will issue requests for a progress report in advance of the review date, and continued approval will be contingent on an adequate response.
Further, LSU requires all researchers (students and faculty) to read and sign the data security form (see link on right). No applications will be approved without the signed agreement.
LSU also requires all researchers (students and faculty) to complete the CITI Program online human subjects research training in either social and behavioral research or biomedical research (see training link on right). It takes about four hours. Upon successfully completing the course, you will receive an electronic certificate, which you’ll need to share with the IRB. No IRB applications will be approved until certificates are obtained.
All inquiries for the IRB should be directed to Dr. Alex Cohen—see information below.
Alex Cohen, PhD, Chair
Douglas Villien, Compliance Specialist
131 David Boyd Hall
Louisiana State University
Baton Rouge, LA 70803