Avoid delays by understanding the IRB process from protocol submission to review, revision, and appr...
Search
70
results
Filter by type
Filter by office
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
Some federal agencies, specifically NIH, NSF, and USDA-NIFA, carry special requirements for tra...
Federal requirements for training on sponsored research awards are changing. To keep Cornell’s resea...
Responsible Conduct of Research is a crucial component of the education provided to students and tra...