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–13
Requires the Secretary to set up an Interagency Coordinating Committee on Newborn and Child Screening to study current programs and systems and to make recommendations. The committee must recommend programs to collect, analyze, and share data on the heritable disorders the Advisory Committee on Heritable Disorders in Newborns and Children recommends (including how often they occur and the bad health outcomes they cause). It must also recommend creating regional centers to study what interventions work and to give public information and education. The committee must include the CDC Director, the HRSA Administrator, the AHRQ Director, the FDA Commissioner, and the NIH Director (or their designees). It must report its recommendations to the Secretary and the relevant Congressional committees and do other tasks the Secretary assigns.
Full Legal Text
The Public Health and Welfare — Source: USLM XML via OLRC
Legislative History
Reference
Citation
42 U.S.C. § 300b–13
Title 42 — The Public Health and Welfare
Last Updated
Apr 6, 2026
Release point: 119-73