§300b–10. Advisory Committee on Heritable Disorders in Newborns and Children — Inbound Citations

Citations to 42 U.S.C. § 300b–10 as a whole

• 42 U.S.C. § 300b–11(a)(3)

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  (3) maintain current information on quality indicators to measure performance of newborn screening, such as false-positive rates and other quality indicators as determined by the Advisory Committee under section 300b–10 of this title;
• 42 U.S.C. § 300b–12(a)

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  (a) The Secretary, acting through the Director of the Centers for Disease Control and Prevention and taking into consideration the expertise of the Advisory Committee on Heritable Disorders in Newborns and Children established under section 300b–10 of this title, shall provide for—

  (1) quality assurance for laboratories involved in screening newborns and children for heritable disorders, including quality assurance for newborn-screening tests, timeliness for processing such tests, performance evaluation services, and technical assistance and technology transfer to newborn screening laboratories to ensure analytic validity and utility of screening tests; and

  (2) appropriate quality control and other performance test materials to evaluate the performance of new screening tools.
• 42 U.S.C. § 300b–12(b)

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  (b) The Secretary, acting through the Director of the Centers for Disease Control and Prevention, and taking into consideration the expertise of the Advisory Committee on Heritable Disorders in Newborns and Children established under section 300b–10 of this title, may provide, as appropriate, for the coordination of surveillance activities, including—

  (1) through standardized data collection and reporting, as well as the use of electronic health records; and

  (2) by promoting data sharing regarding newborn screening with State-based birth defects and developmental disabilities monitoring programs.
• 42 U.S.C. § 300b–13(a)(1)

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  (1) assess existing activities and infrastructure, including activities on birth defects and developmental disabilities authorized under section 247b–4 of this title, in order to make recommendations for programs to collect, analyze, and make available data on the heritable disorders recommended by the Advisory Committee on Heritable Disorders in Newborns and Children under section 300b–10 of this title, including data on the incidence and prevalence of, as well as poor health outcomes resulting from, such disorders; and
• 42 U.S.C. § 300b–16(1)

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  (1) to carry out sections 300b–8, 300b–9, 300b–10, and 300b–11 of this title, $11,900,000 for each of fiscal years 2015 through 2019; and