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This is the charge of the Institutional Review Board (IRB) for research involving human participants...

This is a policy and procedure document for initial, amendment, and continuing review by the IRB inc...

This SOP sets forth the definitions and examples of unanticipated problems (UPs) and adverse events ...

This policy sets forth the definition and examples of noncompliance; the procedures for reporting an...

This policy sets forth which persons/entities have the authority to enact a suspension or terminatio...

The Institutional Official has delegated this reporting authority to the Director of Office of Resea...

This SOP sets forth the requirements for and process by which a PI should close their IRB protocol. ...

The recruitment of human participants for a research study is seen by the IRB as the initial stage o...

The IRB requires investigators to conduct an effective informed consent process with each and every ...

This document sets forth the requirements for obtaining (a) IRB approval of research involving child...