A limited number of biomedical procedures are used in human participant studies on the Ithaca campus...
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Avoid delays by understanding the IRB process from protocol submission to review, revision, and appr...
Guidance provided by the Cornell IRB for identifying and managing compliance for clinical trials inv...
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. ...
Archive of updates on regulations, systems, and expectations from federal sponsors.
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...
Invention is the first formal step in the commercialization process. All inventions made by faculty,...
Per the Final NIH Policy for Data Management and Sharing (NOT-OD-21-013), starting on January 25th, ...