A collection of informed consent, assent, and debriefing templates that can be used for your human p...
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The Cornell IRB is no longer using fillable forms. All protocol-related submissions and other report...
The Cornell IRB is no longer using fillable forms. All protocol-related submissions and other report...
Guidance provided by the Cornell IRB for identifying and managing compliance for clinical trials inv...
This SOP sets forth the requirements for and process by which a PI should close their IRB protocol. ...
This policy serves to help identify who can be the PI of record for an IACUC protocol as defined by ...
The IACUC must review all proposed teaching, testing, and research activities using live vertebrate ...
Institutional Review Board for Human Participant Research (IRB) Office
Institutional Review Board for Human Participant Research (IRB) Office
This document sets forth the additional requirements for obtaining IRB approval for research involvi...