The Cornell IRB is no longer using fillable forms. All protocol-related submissions and other report...
Search
90
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...
Mark Hurwitz, PhD
Chief Research Compliance Officer | Research Integrity Officer | Export Control and Compliance Officer | Research Security OfficerORIA - Office of Research Integrity and Assurance
Export Controls
Research Security Office
This SOP sets forth the requirements for and process by which a PI should close their IRB protocol. ...
ORIA - Office of Research Integrity and Assurance
IRB - Institutional Review Board
Updated: Saturday, March 23, 2024 U.S. Fed Gov remains in standard funded operation, with no impact...
Published on: Monday, September 25, 2023 - 5:45pm
Per the Final NIH Policy for Data Management and Sharing (NOT-OD-21-013), starting on January 25th, ...
Published on: Monday, January 30, 2023 - 12:51pm