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...
IP Series #2: Why are diagnostic claims so hard to get (in the US)?
The IP series features invited guest speakers who will provide an overview of the different types of...
Per the Final NIH Policy for Data Management and Sharing (NOT-OD-21-013), starting on January 25th, ...
March 2023 OSP Roundtable - Export Controls and Academia
An introduction to export control compliance, how export controls apply to academia, and how Cornell...
The Cornell IRB is extending its human participant research training requirement to apply to Cornell...
Institutional Review Board for Human Participant Research (IRB) Office
Institutional Review Board for Human Participant Research (IRB) Office
Updates on regulations, systems, and expectations from federal sponsors. Includes Cornell public com...