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A limited number of biomedical procedures are used in human participant studies on the Ithaca campus...
Avoid delays by understanding the IRB process from protocol submission to review, revision, and appr...
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. ...
Updated: Saturday, March 23, 2024 U.S. Fed Gov remains in standard funded operation, with no impact...
Per the Final NIH Policy for Data Management and Sharing (NOT-OD-21-013), starting on January 25th, ...
Need administrative help for your center? Considering starting a new center? Click "Get Support" abo...
The Cornell IRB is extending its human participant research training requirement to apply to Cornell...