IRB regulations now incorporate the broad definition of “clinical trial” adopted by the National Ins...
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Research with human participants in other countries must comply with both U.S. and international eth...
When Cornell researchers plan to participate in a collaborative or multi-site study, there are a few...
Here you will find answers to frequently asked questions about human participant research at Cornell...
This is an approved guidance document, detailing the role and responsibilities of Conflict Managers,...
Revisions to the Federal policy for the protection of human participants in research (the "Comm...
Learn about the research implications of the General Data Protection Regulation (GDPR).
CONTENTS 1. New NIH Data Sharing and Management Policy 2. RASS-COI –System for Conflicts of Inter...
Beginning January 20, 2020, the Federal Policy for the Protection of Human Subjects (the “Common Rul...