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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...

Federal and state regulations mandate that research involving human participants must be reviewed an...

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 ...

This page contains information for researchers and research participants on how and when to report s...

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...