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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...

Greetings, Cornell research community! We hope your semester is off to a promising start. As we move...

FERPA—the Family Educational Rights and Privacy Act—is a federal law that protects the privacy ...

Below you can find all announcements & newsletters that have been sent to IRB researchers since ...

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...