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. ...
Conflict of Interest (COI) Office
Conflict of Interest (COI) Office
Per the Final NIH Policy for Data Management and Sharing (NOT-OD-21-013), starting on January 25th, ...
Fillable form for use in creating an NSF Safe and Inclusive Working Environments Plan.
The National Science Foundation (NSF) has published revisions to their core policy documents that re...
The Cornell IRB is extending its human participant research training requirement to apply to Cornell...