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Many sponsors—as well as research compliance committees (such as the IRB)—require data management pl...

Once your research project is complete, you will likely have a number of files (hard copy and electr...

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...

Here you will find answers to frequently asked questions about human participant research at Cornell...

Members of the Cornell University community are expected to perform their scholarly and scientific a...