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. ...
ORIA - Office of Research Integrity and Assurance
IRB - Institutional Review Board
IBC - Institutional Biosafety Committee
ORIA - Office of Research Integrity and Assurance
Schedules for IBC meetings and MUA submission deadline