Newborn Screening Saves Lives Reauthorization Act of 2019

Summary

Newborn Screening Saves Lives Reauthorization Act of 2019 This bill reauthorizes through FY2024 and revises several programs and activities relating to newborn screening for genetic diseases. Among other things, the bill reauthorizes, and makes mandatory rather than discretionary, the Hunter Kelly Research Program at the National Institutes of Health as well as national surveillance activities conducted by the Centers for Disease Control and Prevention.

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Documents

10 official files

• Referred in Senate (text)

  Referred in Senate · EN · 25 July 2019

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• Referred in Senate (PDF)

  Referred in Senate · EN · 25 July 2019

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• Engrossed in House (text)

  Engrossed in House · EN · 24 July 2019

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• Engrossed in House (PDF)

  Engrossed in House · EN · 24 July 2019

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• Passed House

  summary · EN · 24 July 2019

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• Reported in House (text)

  Reported in House · EN · 23 July 2019

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• Reported in House (PDF)

  Reported in House · EN · 23 July 2019

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• Introduced in House (text)

  Introduced in House · EN · 2 May 2019

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• Introduced in House (PDF)

  Introduced in House · EN · 2 May 2019

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• Introduced in House

  summary · EN · 2 May 2019

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