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...
Many sponsors—as well as research compliance committees (such as the IRB)—require data management pl...
Once your research project is complete, you will likely have a number of files (hard copy and electr...
Some federal agencies, specifically NIH, NSF, and USDA-NIFA, carry special requirements for tra...
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...
Schedules for IBC meetings and MUA submission deadline
Invention is the first formal step in the commercialization process. All inventions made by faculty,...
Federal requirements for training on sponsored research awards are changing. To keep Cornell’s resea...