All human subjects research connected with members of the Smith College community (either as researchers or study participants) must be reviewed and approved by the IRB prior to the initiation of the ...

Due to the involved nature of the IRB review process, submitting research projects for review can prove to be challenging. In order to simplify the process and support investigators, the IRB has ...

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 ...

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 ...

Below is a list of guidance/policies developed by the W&M IRB. To find specific guidance, you can use the "control F" (Dell computers) or "command F" (Mac computers) feature on your computer to search ...

Follow the step-by-step instructions below to successfully maintain and close a protocol with the IRB. Instructions below include information about continuing reviews, amendments, event reporting (new ...

The Federal Policy for the Protection of Human Subjects or the “Common Rule” outlines specific regulations for human subjects research. The Common Rule is heavily based on the "The Belmont Report," ...

Migration of Institutional Review Board (IRB) activities to the Purdue Excellence in Research Administration (PERA) platform is underway. The PERA-IRB module will go live Monday (Oct. 27). With the ...

It is important for researchers to understand how to use an external IRB as the IRB of record, as well as what is required throughout the process. This UB CTSI Watch and Learn educational module video ...

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 ...