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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. ...
Responsible Conduct of Research (RCR) Office
Responsible Conduct of Research (RCR) Office
Mark Hurwitz (Interim)
Director of Research Integrity and Security | Export Control and Compliance OfficerExport Controls
ORIA - Office of Research Integrity and Assurance
RCR - Responsible Conduct of Research
COI - Conflict of Interest
Some federal agencies, specifically NIH, NSF, and USDA-NIFA, carry special requirements for tra...