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...
Cornell provides a secure registry system for faculty, staff, and students to record Cornell-related...
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. ...
To safeguard the reputations of Cornell researchers, Cornell, and external sponsors, it is important...
The Creating Helpful Incentives to Produce Semiconductors (CHIPS) and Science Act of 2022 prohibits ...
Some federal agencies, specifically NIH, NSF, and USDA-NIFA, carry special requirements for tra...