Title 42 › Chapter 6A— PUBLIC HEALTH SERVICE › Subchapter IX— GENETIC DISEASES, HEMOPHILIA PROGRAMS, AND SUDDEN INFANT DEATH SYNDROME › Part A— Genetic Diseases › § 300b–8
The Secretary, using money set aside under section 300b–16 and working through the Health Resources and Services Administration (and with advice from the Advisory Committee on Heritable Disorders in Newborns and Children), must give grants to eligible groups to make newborn and child screening better. Grants can be used to help state and local health agencies offer screening, counseling, and care; train health and lab staff on new testing methods, fast handling of samples, and sharing info with families and doctors; create easy-to-understand education for parents and support groups; set up or run systems to track follow-up and treatment; and speed up sample handling and diagnosis. Eligible groups include states or local governments, multi-state teams, territories, Indian Health Service programs or facilities, and other groups with relevant newborn screening expertise. Applicants must promise they have adopted, are adopting, or will use the grant to adopt and follow the Advisory Committee’s guidelines that the Secretary has approved, including screening every newborn for the disorders those guidelines recommend. The Secretary must coordinate these grants with other newborn screening work and give technical help as needed. Grants cannot be used for cash payments to affected people, inpatient services, buying land or major property improvements, or for proprietary research or training. Participation in programs funded by these grants must be voluntary. Grant money must add to, not replace, other federal, state, or local funds. States must publish grant applications for public comment and address any comments they get.
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The Public Health and Welfare, Source: USLM XML via OLRC
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42 U.S.C. § 300b–8
Title 42, The Public Health and Welfare
Last Updated
Apr 5, 2026
Release point: 119-73not60