The University of Iowa

Part 1, Ch. 7 - Regulatory Requirements for IRB Review

Manuals

The Department of Health and Human Services via the Office for Human Research Protections and the Food and Drug Administration among others provide the regulatory framework for the conduct of human subjects research and human subjects research protections.  The department’s respective regulations were modified in 1981 to be compatible; the Federal Policy for the Protection of Human Subjects or the “Common Rule” was published in 1991.