This Congressionally mandated group was formed in November 1978, by Public Law 95-622, succeeding the
National Commission for the Protection of Human Subjects of Biomedical and Behavioral Research. It was created to study bio-ethical issues such as the effects of income and residence on the availability of healthcare, the definition of death, patient consent, human research subjects, and genetic engineering, counseling and testing. and ultimately published 11 reports, two of which were made up of three volumes, on these topics and their implications. These reports expanded upon ideas originally established in the 1945
Nuremberg Codes and the
Belmont Report. Additionally, a guidebook for
Institutional Review Boards was published by the commission in 1981. == History ==