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...
National Security Presidential Memorandum-33 (NSPM-33) directs federal agencies and departments to f...
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.