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. ...
This page consists of a series of Frequently asked questions about materials used in research that r...
All research that involves the use of human embryonic stem cells, human embryos, or their derivative...
Schedules for IBC meetings and MUA submission deadline
Looking for guidance and resources? The links and documents below will help you to understand the ma...
Federal and state regulations mandate that research involving human participants must be reviewed an...
To report an incident or exposure Cornell University Injury/Illness/Exposure Report