Responsible Conduct of Research is a crucial component of the education provided to students and tra...
Search
187
results
Filter by type
Filter by office
A collection of informed consent, assent, and debriefing templates that can be used for your human p...
The Cornell IRB is no longer using fillable forms. All protocol-related submissions and other report...
The Cornell IRB is no longer using fillable forms. All protocol-related submissions and other report...
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