Title 42 › Chapter CHAPTER 6A— - PUBLIC HEALTH SERVICE › Subchapter SUBCHAPTER IX— - GENETIC DISEASES, HEMOPHILIA PROGRAMS, AND SUDDEN INFANT DEATH SYNDROME › Part Part A— - Genetic Diseases › § 300b–8
The Secretary must give grants, using money from section 300b–16, through the Health Resources and Services Administration Administrator and with advice from the Advisory Committee on Heritable Disorders in Newborns and Children. The grants must help eligible groups strengthen newborn and child screening programs, train health and lab workers in new screening technology and timely specimen handling, teach families and support groups about screening and follow-up at appropriate reading levels, build systems to track and coordinate follow-up and treatment, and speed up specimen testing and diagnosis. An eligible entity can be a State or its local government, a group of 2 or more States or local governments, a U.S. territory, an Indian Health Service facility or program, or another group the Secretary approves. Applicants must promise to follow the Advisory Committee’s guidelines that the Secretary has adopted, including screening every newborn for the recommended disorders. The Secretary must coordinate these programs and give technical help. Grant funds may not be used for cash payments to patients, inpatient care, buying land or major building work, or proprietary research or training. Participation must be voluntary, funds must add to (not replace) other public money, and grant applications must be made public for comment and respond to those comments.
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The Public Health and Welfare — Source: USLM XML via OLRC
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Citation
42 U.S.C. § 300b–8
Title 42 — The Public Health and Welfare
Last Updated
Apr 6, 2026
Release point: 119-73