The Cornell IRB is no longer using fillable forms. All protocol-related submissions and other report...
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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. ...
Register for the federal and non-federal systems used for identifying potential funding sources and ...
Per the Final NIH Policy for Data Management and Sharing (NOT-OD-21-013), starting on January 25th, ...
Recommended documentation and training for unit research administrators. Includes courses, contacts,...
If you are conducting research with human participants (e.g., surveys, interviews, blood draws, seco...
The Cornell IRB is extending its human participant research training requirement to apply to Cornell...