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Guidance provided by the Cornell IRB for identifying and managing compliance for clinical trials inv...
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 ...
Looking for guidance and resources? The links and documents below will help you to understand the ma...
Federal and state regulations mandate that research involving human participants must be reviewed an...
This document sets forth the additional requirements for obtaining IRB approval for research involvi...
This resource is intended to guide Cornell researchers through the process of submitting, modifying,...
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