The OIRB and the UAB IRBs are fully operational. OIRB staff are part of the UAB Workgroup A, Group 2, which means they continue to work remotely during UAB’s announced modified business operations.

When is IRB Approval Required? If your project involves "research" and "human subjects" as defined by 45 CFR 46, you must submit an application to the Case Western Reserve University Institutional ...

The University IRB has the authority to suspend or terminate IRB approval of research that is not being conducted in accordance with IRB requirements or that may pose unexpected, serious harm to ...

The mission of Pratt Institute’s Human Research Subjects Committee / Institutional Review Board (IRB) is to ensure quality research involving human subjects conducted under the auspices of the ...

Single IRB Review is an arrangement in which one institution's IRB provides review, approval and oversight for the Human Research activities of multiple institutions. This is intended to streamline ...

These collected resources can help when you're developing IRB protocols and related materials. If you have further questions after reviewing these materials, please contact our office. We also ...

For your convenience, below is information about the IRB. Forms and processes for IRB submission are online. An overview on regulatory binder preparation and maintenance can be found in a presentation ...

There is often confusion as to which classroom projects and independent student projects must be reviewed by the Institutional Review Board. Generally, a student project involving human subjects falls ...

The committee reviews and approves research and training materials related to the derivation and use of pHSCs, including human embryonic stem cells (hESC) and pluripotent stem cells produced from ...

The University considers an external IRB to be any IRB that is not the University IRB (i.e., the local IRB) including: Independent IRB: a review board that is not owned or operated by the research ...

A single IRB (sIRB) of record will be used in the ethical review of non-exempt human subjects research protocols funded by federal agencies that are carried out at more than one site in the United ...