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–15
Carry out and grow a newborn screening research program called the Hunter Kelly Newborn Screening Research Program. The program can develop and test better screening tools, work on experimental treatments and care for extra newborn conditions and other genetic or metabolic problems found by newborn screening, give research data for conditions the Advisory Committee is reviewing to be added to the recommended screening list, run pilot studies so new screenings are ready for the whole country, and do other improvements the NIH Director finds useful. "Additional newborn condition" means any condition not on the core recommended list the Secretary adopted. Groups that get program money must, when possible, consult state health departments and focus on testing methods not already used in their state and on conditions on the recommended screening panel. The NIH Director is encouraged to include program activities in the required two-year report and share that information on the Internet clearinghouse. The program must avoid duplicating work, add to but not replace existing efforts, and must not interfere with the NIH peer-review process.
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The Public Health and Welfare — Source: USLM XML via OLRC
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42 U.S.C. § 300b–15
Title 42 — The Public Health and Welfare
Last Updated
Apr 6, 2026
Release point: 119-73