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...
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.
Schedules for IBC meetings and MUA submission deadline
Invention is the first formal step in the commercialization process. All inventions made by faculty,...
Per the Final NIH Policy for Data Management and Sharing (NOT-OD-21-013), starting on January 25th, ...