This SOP sets forth the requirements for and process by which a PI should close their IRB protocol. ...
Policies
The recruitment of human participants for a research study is seen by the IRB as the initial stage o...
Guidance provided by the Cornell IRB for identifying and managing compliance for clinical trials inv...
Guidance from the Cornell IRB on developing an oral consent script, for those studies where a writte...
Guidance from the Cornell IRB and Environmental Health and Safety on common hygiene practices to use...
The Cornell Office of Research Integrity and Assurance (ORIA) has developed guidance relevant to res...
Guidance provided by the Cornell IRB on different types of reviews that may be required for internat...
Guidance from the Cornell IRB on the types of studies that could result in the identification of res...
Per the Notice of Changes to NIH Policy for Issuing Certificates of Confidentiality (NOT-OD-17-109),...
Guidance provided by the Cornell IRB for determining whether or not IRB review and approval is neede...