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IRB regulations now incorporate the broad definition of “clinical trial” adopted by the National Ins...

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...

On this page you will find answers to commonly asked questions pertaining to Cornell IRB office func...

Cornell’s Individual Standard Non-Disclosure Agreement (NDA) is a mechanism by which a Cornell emplo...