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Looking for guidance and resources? The links and documents below will help you to understand the ma...
Institutional Review Board for Human Participant Research (IRB) Office
Institutional Review Board for Human Participant Research (IRB) Office
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. ...
To safeguard the reputations of Cornell researchers, Cornell, and external sponsors, it is important...
Archive of updates on regulations, systems, and expectations from federal sponsors.