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United States · Bill · HR

H.R. 2951 (112th)

Patients First Act of 2011

referredUnited States· United States Congress· EN

Introduced

15 September 2011

Last action

20 September 2011 · Referred

Status

Referred to the Subcommittee on Health.

Sponsors

Rep. Forbes, J. Randy [R-VA-4], Rep. Lipinski, Daniel [D-IL-3], Rep. Smith, Christopher H. [R-NJ-4], Rep. Coffman, Mike [R-CO-6], Rep. Franks, Trent [R-AZ-8], Rep. Lamborn, Doug [R-CO-5], Rep. Hensarling, Jeb [R-TX-5], Rep. Schmidt, Jean [R-OH-2], Rep. Westmoreland, Lynn A. [R-GA-3], Rep. Pitts, Joseph R. [R-PA-16], Sen. Blackburn, Marsha [R-TN], Rep. Ellmers, Renee L. [R-NC-2], Rep. Latta, Robert E. [R-OH-5], Rep. Canseco, Francisco "Quico" [R-TX-23], Rep. Pence, Mike [R-IN-6], Rep. Nunnelee, Alan [R-MS-1], Rep. Wittman, Robert J. [R-VA-1], Rep. Miller, Jeff [R-FL-1], Rep. Huelskamp, Tim [R-KS-1], Rep. Fleming, John [R-LA-4], Rep. Huizenga, Bill [R-MI-4], Rep. Roe, David P. [R-TN-1], Rep. Landry, Jeffrey M. [R-LA-3], Rep. Austria, Steve [R-OH-7], Rep. Boustany, Charles W., Jr. [R-LA-3], Rep. Johnson, Bill [R-OH-6], Rep. Hartzler, Vicky [R-MO-4], Rep. King, Steve [R-IA-4], Rep. Ross, Dennis A. [R-FL-15], Sen. Lankford, James [R-OK], Rep. Black, Diane [R-TN-6]

Subjects

Healthcare

Source updated

14 August 2025

Healthcare

Summary

Patients First Act of 2011 - Amends the Public Health Service Act to require the Secretary of Health and Human Services to conduct and support basic and applied research to develop techniques for the isolation, derivation, production, testing, and human clinical use of stem cells that may result in improved understanding of, or treatments for, diseases and other adverse health conditions, including pluripotent stem cells that have the flexibility of embryonic stem cells (whether or not such pluripotent stem cells have an embryonic source), provided that such techniques will not involve: (1) the creation of a human embryo for research purposes; (2) the destruction or discarding of, or risk of injury to, a living human embryo; or (3) the use of any stem cell the derivation or provision of which would be inconsistent with this Act. Requires the Secretary to issue guidelines implementing this Act to ensure that any research (including any clinical trial) supported under this Act: (1) is clearly consistent with the standards established in this Act, if conducted using human cells; and (2) is prioritized in terms of potential for near-term clinical benefit in human patients. Requires the Secretary to report on peer reviewed stem cell research proposals that were not funded.

This text is taken from the official record. PoliticalRepo does not editorialize.

Timeline

  1. 15 September 2011

    Introduced

    Referred to the House Committee on Energy and Commerce.

    Source: IntroReferral

  2. 15 September 2011

    Introduced

    Introduced in House

    Source: IntroReferral

  3. 15 September 2011

    Introduced

    Introduced in House

    Source: IntroReferral

  4. 20 September 2011

    Referred

    Referred to the Subcommittee on Health.

    Source: Committee

Votes

No vote records are attached yet.

Versions

Documents

3 official files

Introduced in House (text)

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  • Introduced in House (text)

    Introduced in House · EN · 15 September 2011

    ViewDownloadOpen at official source

  • Introduced in House (PDF)

    Introduced in House · EN · 15 September 2011

    ViewDownloadOpen at official source

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  • Introduced in House

    summary · EN · 15 September 2011

    Open at official source

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Sponsors

Related records

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Sources

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