The Cornell IRB is no longer using fillable forms. All protocol-related submissions and other report...
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A collection of informed consent, assent, and debriefing templates that can be used for your human p...
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. ...
Per the Final NIH Policy for Data Management and Sharing (NOT-OD-21-013), starting on January 25th, ...
The Cornell IRB is extending its human participant research training requirement to apply to Cornell...
This document sets forth the additional requirements for obtaining IRB approval for research involvi...