The goal of the informed consent process is to ensure that the research subject is treated with respect and human dignity. The process does this by safeguarding and advocating for the subject's right ...

In response to user feedback regarding the CoeusLite IRB (Institutional Review Board) experience, the following submission processes have been updated: * Exempt Request. * Study Amendment, including ...

Note that all forms must be completed on a computer. No handwritten forms will be accepted for review. Before you take the time to prepare your application, you want to make sure the project you are ...

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 ...

Any research that involves human subjects, whether funded or not, that is undertaken by a WIU faculty, academic staff or student or supported by Western Illinois University, must be reviewed by the ...

The UAB Institutional Review Board for Human Use (IRB) is a committee established under federal regulations for the protection of human subjects in research (45 CFR 46). Its purpose is to help protect ...

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 ...

Investigational use of a Humanitarian Use Device (i.e., to establish safety and effectiveness of the device, regardless of whether it is being used in accordance with its Humanitarian Device Exemption ...

The sample consent forms are being provided to you as a tool. They contain all of the required elements of an acceptable consent form. While we strongly recommend that you follow the format that we ...

A modification request is required if you plan to make any changes to your research or deviate from the protocol after approval or exemption has been granted. Such changes include, but are not limited ...