The Federal Policy for the Protection of Human Subjects or the “Common Rule” outlines specific regulations for human subjects research. The Common Rule is heavily based on the "The Belmont Report," ...

The Food and Drug Administration ("FDA") expands informed consent exceptions with a final rule permitting institutional review board ("IRB") waiver or alteration of elements for certain FDA-regulated ...

The Common Rule describes the basic DHHS policy for the protection of human research participants and is incorporated into University policy for: IRB review types and processes; criteria for IRB ...

This resources lists hyperlinks to federal resources that are useful to researchers getting started in human subjects research. The Federal Policy for the Protection of Human Subjects or the “Common ...