The Cornell IRB is no longer using fillable forms. All protocol-related submissions and other report...
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The Cornell IRB is no longer using fillable forms. All protocol-related submissions and other report...
Once your research project is complete, you will likely have a number of files (hard copy and electr...
A collection of informed consent, assent, and debriefing templates that can be used for your human p...
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...
Beginning January 20, 2020, the Federal Policy for the Protection of Human Subjects (the “Common Rul...
Published on: Friday, January 17, 2020 - 3:41pm
ORIA - Office of Research Integrity and Assurance
IRB - Institutional Review Board
OSP - Office of Sponsored Programs & Research Development
Pre-Award Research Operations (PRO) Team