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...
Cornell’s Export Control Office performs periodic outreach, self-audits, and risk assessment activit...
The Cornell University Export Control Compliance manual is available from this site as a PDF.
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, ...
It is critical that faculty, staff and students wishing to travel to Iran or engage with an Iranian ...
The Cornell IRB is extending its human participant research training requirement to apply to Cornell...