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 federal government will give grants through the Health Resources and Services Administration (HRSA). These grants help states and other groups make newborn and child screening better. Grants can pay to expand screening and follow-up services, train health care and lab staff on new testing methods and quick handling of samples, teach parents and groups about screening and care, set up systems to track and coordinate follow-up and treatment, and speed up diagnosis. Eligible groups include: a State or local government; a group of two or more States or local governments; a U.S. territory; a health program run by or under contract with the Indian Health Service; and other organizations with newborn screening expertise. To get a grant, an applicant must follow the Advisory Committee’s recommended screening guidelines that the Secretary has adopted, including testing for the disorders the Committee recommends. Grants must be coordinated with existing programs. Grant money cannot be used for cash payments to people, inpatient hospital care, buying land or major building projects, or private proprietary research or training. Participation must be voluntary. Applications must be made public for comment and the Secretary will give technical help to grantees.
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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
Sep 22, 2026
Release point: 119-110