Title 42 › CHAPTER 6A — PUBLIC HEALTH SERVICE › SUBCHAPTER IX — GENETIC DISEASES, HEMOPHILIA PROGRAMS, AND SUDDEN INFANT DEATH SYNDROME › Part A — Genetic Diseases › § 300b–13
Create an Interagency Coordinating Committee on Newborn and Child Screening to review current programs and systems, including work on birth defects and developmental disabilities, and to recommend programs to collect, analyze, and share data on heritable disorders the Advisory Committee recommends. It must report how often these disorders happen, the poor health outcomes they cause, and suggest regional centers to study ways to prevent those outcomes and to inform the public. The Secretary must set up the committee. Members must include the heads or designees of CDC, HRSA, AHRQ, FDA, and NIH. The committee must send its recommendations to the Secretary and to relevant congressional committees and do other work the Secretary finds appropriate.
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The Public Health and Welfare, Source: USLM XML via OLRC
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42 U.S.C. § 300b–13
Title 42, The Public Health and Welfare
Last Updated
Sep 22, 2026
Release point: 119-110