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...
Mark Hurwitz, PhD
Chief Research Compliance Officer | Research Integrity Officer | Export Control and Compliance Officer | Research Security OfficerOnce 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. ...
Register for the federal and non-federal systems used for identifying potential funding sources and ...
To safeguard the reputations of Cornell researchers, Cornell, and external sponsors, it is important...
The Creating Helpful Incentives to Produce Semiconductors (CHIPS) and Science Act of 2022 prohibits ...