This is a guidance document to help researchers prepare applications to the IRB that involve the use...
Policies
This is a guidance document for initial and continuing review by the IRB including requirements for ...
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...
Guidance provided by the Cornell IRB for identifying and managing compliance for clinical trials inv...
Guidance from the Cornell IRB on developing an oral consent script, for those studies where a writte...