S. 1858 (110th): Newborn Screening Saves Lives Act of 2007

Introduced:
Jul 23, 2007 (110th Congress, 2007–2009)
Status:
Signed by the President
Slip Law:
This bill became Pub.L. 110-204.
Sponsor
Christopher Dodd
Senator from Connecticut
Party
Democrat
Text
Read Text »
Last Updated
Apr 30, 2008
Length
8 pages
Related Bills
S. 2663 (109th) was a previous version of this bill.

Referred to Committee
Last Action: Apr 27, 2006

H.R. 3825 (identical)

Reported by Committee
Last Action: Mar 13, 2008

 
Status

This bill was enacted after being signed by the President on April 24, 2008.

Progress
Introduced Jul 23, 2007
Referred to Committee Jul 23, 2007
Reported by Committee Nov 14, 2007
Passed Senate Dec 13, 2007
Passed House Apr 08, 2008
Signed by the President Apr 24, 2008
 
Full Title

A bill to amend the Public Health Service Act to establish grant programs to provide for education and outreach on newborn screening and coordinated followup care once newborn screening has been conducted, to reauthorize programs under part A of title XI of such Act, and for other purposes.

Summary

No summaries available.

Cosponsors
21 cosponsors (15D, 5R, 1I) (show)
Committees

House Energy and Commerce

Health

Senate Health, Education, Labor, and Pensions

The committee chair determines whether a bill will move past the committee stage.

 
Primary Source

THOMAS.gov (The Library of Congress)

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Notes

S. stands for Senate bill.

A bill must be passed by both the House and Senate in identical form and then be signed by the president to become law.

GovTrack’s Bill Summary

We don’t have a summary available yet.

Library of Congress Summary

The summary below was written by the Congressional Research Service, which is a nonpartisan division of the Library of Congress.


4/24/2008--Public Law.
Newborn Screening Saves Lives Act of 2007 -
Section 2 -
Amends the Public Health Service Act to authorize the Secretary of Health and Human Services, acting through the Administrator of the Health Resources and Services Administration (HRSA), to award grants to eligible entities to:
(1) provide screening, counseling, or health care services to newborns and children having or at risk for heritable disorders;
(2) provide education and training in newborn screening and congenital, genetic, and metabolic disorders to health care professionals and newborn screening laboratory personnel;
(3) develop and deliver educational programs about newborn screening, counseling, testing, follow-up, treatment, and specialty services to parents, families, and patient advocacy and support groups; and
(4) establish, maintain, and operate a system to assess and coordinate treatment relating to congenital, genetic, and metabolic disorders.
Section 3 -
Authorizes appropriations for FY2008-FY2012 for grants for demonstration programs to evaluate the effectiveness of screening, counseling, or health care services in reducing the morbidity and mortality caused by heritable disorders in newborns and children.
Section 4 -
Expands the duties of the Advisory Committee on Heritable Disorders in Newborns and Children to include: (1) making recommendations that include the heritable disorders for which all newborns should be screened; (2) developing a model decision-matrix for newborn screening expansion; and (3) considering ways to ensure that all states attain the capacity to screen for the recommended conditions. Sets forth deadlines for the Secretary to make a decision on Advisory Committee recommendations.
Requires the Advisory Committee to continue to operate during the five-year period beginning on the date of enactment of this Act.
Section 5 -
Requires the Secretary, acting through the Administrator, to establish and maintain a central clearinghouse of current information on newborn screening.
Sets forth requirements for such clearinghouse, including:
(1) ensuring that the clearinghouse is available on the Internet and is updated at least quarterly;
(2) providing links to websites that have expertise in newborn screening;
(3) providing information about newborn conditions and screening services available in each state;
(4) providing current research on conditions for which newborn screening tests are available; and
(5) providing the availability of federal funding for newborn and child screening for heritable disorders.
Section 6 -
Requires the Secretary, acting through the Director of the Centers for Disease Control and Prevention (CDC), to provide for: (1) quality assurance for screening laboratories; and (2) appropriate quality control and other performance test materials to evaluate the performance of new screening tools.
Requires the Secretary to establish an Interagency Coordinating Committee on Newborn and Child Screening to make recommendations on: (1) programs to collect, analyze, and make available data on certain heritable disorders; and (2) the establishment of regional centers to conduct applied epidemiological research on effective interventions for preventing poor health outcomes resulting from such disorders and to provide information and education to the public on such effective interventions.
Section 7 -
Requires the Secretary, acting through the Director of CDC, to develop a national contingency plan for newborn screening in the event of a public health emergency.
Authorizes the Secretary to continue to carry out, coordinate, and expand research in newborn screening (to be known as the Hunter Kelly Newborn Screening Research Program), including: (1) identifying, developing, and testing the most promising new screening technologies; and (2) experimental treatments and disease management strategies for conditions that can be detected through newborn screening for which treatment is not yet available.

House Republican Conference Summary

The summary below was written by the House Republican Conference, which is the caucus of Republicans in the House of Representatives.


No summary available.

House Democratic Caucus Summary

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