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S.634
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.
Sponsor: Sen Dodd, Christopher J. [CT] (introduced 2/15/2007) Cosponsors (16)
Related Bills: H.R.1634, S.1858
Latest Major Action: 2/15/2007 Referred to Senate committee. Status: Read twice and referred to the Committee on Health, Education, Labor, and Pensions.
Note: For further action, see S.1858, which became Public Law 110-204 on 4/24/2008.
SUMMARY AS OF:
2/15/2007--Introduced.
Newborn Screening Saves Lives Act of 2007 - Amends the Public Health Service Act to require the Secretary of Health and Human Services, acting through the Associate Administrator of the Maternal and Child Health Bureau of the Health Resources and Services Administration (HRSA), to awards grants to eligible entities to: (1) provide education and training in newborn screening and congenital, genetic, and metabolic disorders to health care professionals and newborn screening laboratory personnel; (2) develop educational programs about newborn screening for parents, families, and patient advocacy and support groups; and (3) establish operate a system to assess and coordinate treatment relating to congenital, genetic, and metabolic disorders.
Requires the Secretary, acting through the Director of the Centers for Disease Control and Prevention (CDC), to develop a national contingency plan for newborn screening for use in the event of a public health emergency.
Requires the Advisory Committee on Heritable Disorders in Newborns and Children to: (1) recommend a uniform screening panel for newborn screening programs that includes the heritable disorders for which all newborns should be screened; and (2) develop a model decision-matrix for newborn screening program expansion. Directs the Secretary to adopt or reject recommendations by the Advisory Committee.
Requires the Secretary, acting through the Director of CDC, to: (1) provide for quality assurance for screening laboratories; (2) provide for population-based pilot testing for evaluating new screening tools; (3) collect, analyze, and make available data on certain heritable disorders; and (4) operate regional centers for the conduct of applied epidemiological research on the prevention of such disorders.
MAJOR ACTIONS:
***NONE***
ALL ACTIONS:
- 2/15/2007:
- Sponsor introductory remarks on measure. (CR S2082)
- 2/15/2007:
- Read twice and referred to the Committee on Health, Education, Labor, and Pensions. (text of measure as introduced: CR S2083-2085)
TITLE(S): (italics indicate a title for a portion of a bill)
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COSPONSORS(16), ALPHABETICAL [followed by Cosponsors withdrawn]: (Sort: by date)
Sen Bayh, Evan [IN] - 3/28/2007
Sen Bingaman, Jeff [NM] - 3/5/2007
Sen Bond, Christopher S. [MO] - 3/23/2007
Sen Brown, Sherrod [OH] - 2/16/2007
Sen Clinton, Hillary Rodham [NY] - 3/6/2007
Sen Cochran, Thad [MS] - 3/12/2007
Sen Coleman, Norm [MN] - 3/5/2007
Sen Durbin, Richard [IL] - 2/28/2007
Sen Hatch, Orrin G. [UT] - 2/15/2007
Sen Johnson, Tim [SD] - 5/3/2007
Sen Kerry, John F. [MA] - 5/24/2007
Sen Lincoln, Blanche L. [AR] - 4/16/2007
Sen Lugar, Richard G. [IN] - 2/27/2007
Sen Murkowski, Lisa [AK] - 3/5/2007
Sen Sanders, Bernard [VT] - 2/16/2007
Sen Schumer, Charles E. [NY] - 3/1/2007
COMMITTEE(S):
| Committee/Subcommittee: | Activity: | |
| Senate Health, Education, Labor, and Pensions | Referral, In Committee | |
RELATED BILL DETAILS: (additional related bills may be indentified in Status)
AMENDMENT(S):
***NONE***