Guidance provided by the Cornell IRB for identifying and managing compliance for clinical trials inv...
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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. ...
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,...
This page consists of a series of Frequently asked questions about materials used in research that r...
All research that involves the use of human embryonic stem cells, human embryos, or their derivative...
Schedules for IBC meetings and MUA submission deadline
Looking for guidance and resources? The links and documents below will help you to understand the ma...
Federal and state regulations mandate that research involving human participants must be reviewed an...