The Cornell IRB is no longer using fillable forms. All protocol-related submissions and other report...
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The Cornell IRB is no longer using fillable forms. All protocol-related submissions and other report...
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...
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. ...
To safeguard the reputations of Cornell researchers, Cornell, and external sponsors, it is important...