Requires the Secretary of Health and Human Services to review all such regulations to harmonize them where feasible with a subsequent proposed rule, explaining remaining differences.
Sets forth the authority of the Secretary to modify regulations.
Requires informed consent, as specified.
Requires an Institutional Review Board to approve all human subject research proposals.
Directs the Secretary to establish criteria for identifying and monitoring high risk clinical trials.
Prohibits the use of Federal funds for classified human subject research, as specified.
Requires the Secretary to determine whether an entity has violated these requirements, as specified.
Establishes an Office of Human Research Protections within the Office of the Secretary to make grants, conduct research and Institutional Review Board audits (requiring corrective action if necessary), and coordinate Federal efforts. Requires the Director to notify the relevant regulatory agency if deficiencies are found.
Authorizes the Director of such Office to make grants for the development of a model education program.
Requires coordination with the Commissioner of Food and Drugs.
Continues the National Research Protections Act Advisory Committee.
Requires the Secretary to promulgate regulations addressing the participation of people with diminished decisionmaking capacity in human subject research.