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Looking for guidance and resources? The links and documents below will help you to understand the ma...

A limited number of biomedical procedures are used in human participant studies on the Ithaca campus...

Avoid delays by understanding the IRB process from protocol submission to review, revision, and appr...

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...

Learn about Cornell University's requirements for human participant research ethics (IRB) training, ...

Informed consent is more than just a form; it is a process that takes place between researcher and p...

Whether you are working with an existing data set collected by another researcher, storing data you ...

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