The Cornell IRB is no longer using fillable forms. All protocol-related submissions and other report...
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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...
CONTENTS Final Reminder: New Exempt Protocol Training Requirement - Effective 10/1/22 Revi...
Published on: Tuesday, October 11, 2022 - 9:30am
Researchers who work with advanced computing chips, supercomputers, semiconductors, or integrated ci...
Published on: Thursday, October 13, 2022 - 12:27am
Per the Notice of Changes to NIH Policy for Issuing Certificates of Confidentiality (NOT-OD-17-109),...
Are you conducting research with human participants? Do you have a financial relationship with an en...
Cornell’s Export Control Office performs periodic outreach, self-audits, and risk assessment activit...