Sponsors and the government hold the University responsible for ensuring that any conflicts related ...
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Looking for guidance and resources? The links and documents below will help you to understand the ma...
A limited number of biomedical procedures are used in human participant studies on the Ithaca campus...
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...
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...
This SOP sets forth the requirements for and process by which a PI should close their IRB protocol. ...
Register for the federal and non-federal systems used for identifying potential funding sources and ...