Policies

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...

Guidance from the Cornell IRB and Environmental Health and Safety on common hygiene practices to use...

The Cornell Office of Research Integrity and Assurance (ORIA) has developed guidance relevant to res...

Guidance provided by the Cornell IRB on different types of reviews that may be required for internat...