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...
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...
Developing a proposal that includes work with animals, human participants, recombinant or synthetic ...
If you are conducting research with human participants (e.g., surveys, interviews, blood draws, seco...
Looking for guidance and resources? The links and documents below will help you to understand the ma...