For new projects approved by administrative review, only projects that are using an external IRB are to submit updated documentation of Reviewing (external) IRB approval. Principal Investigators (PIs) ...

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 ...

Three types of New Projects may be submitted in IRBNet for Administrative Review: requests for human research determinations, reports of emergency use of a test article, and requests to use an ...

The basis for the single IRB model is to allow multiple sites that are conducting the same protocol to use a single IRB for review, instead of using multiple IRBs to review the research at the sites ...

The purpose of this announcement is to provide you with the Human Research Protection Program (HRPP) plans to implement the revised regulations governing research involving human subjects, the Common ...

All studies conducted through one of the health sciences schools must register each of their studies through the CSR system. Only clinical trials (by NIH definition) conducted through the other ...

If you are conducting research at Boston College in conjunction with another university, hospital, or other institution that has an IRB, you may request an IRB Authorization Agreement (IAA), also ...

This announcement describes updates to the initial form that were published on 11/03/2025. Researchers who created an initial form after the updated form was published will utilize the new form. Added ...

Western Michigan University fosters a research environment to promote respect for the rights and welfare of individuals involved in human subject research. Actions of the university will be guided by ...