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...
Once your research project is complete, you will likely have a number of files (hard copy and electr...
This SOP sets forth the requirements for and process by which a PI should close their IRB protocol. ...
Archive of updates on regulations, systems, and expectations from federal sponsors.
Published on: Wednesday, January 18, 2023 - 2:54pm