Avoid delays by understanding the IRB process from protocol submission to review, revision, and appr...
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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 ...
To safeguard the reputations of Cornell researchers, Cornell, and external sponsors, it is important...
Archive of updates on regulations, systems, and expectations from federal sponsors.
Cornell has developed an online training course on Responsible and Ethical Conduct of Research and R...
Some federal agencies, specifically NIH, NSF, and USDA-NIFA, carry special requirements for tra...