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United States · Bill · HR

H.R. 3627 (109th)

Rapid Pathogen Identification to Delivery of Cures Act

referredUnited States· United States Congress· EN

Introduced

29 July 2005

Last action

19 September 2005 · Referred

Status

Referred to the Subcommittee on Terrorism, Unconventional Threats and Capabilities.

Sponsors

Del. Christensen, Donna M. [D-VI-At Large], Bennie Thompson, Rep. Dicks, Norman D. [D-WA-6], Zoe Lofgren, JAMES LANGEVIN

Subjects

Healthcare, Defence

Source updated

15 August 2025

Healthcare · Defence

Summary

Rapid Pathogen Identification to Delivery of Cures Act - Amends the Homeland Security Act of 2002 to require the Secretary of Homeland Security to submit a report setting forth a strategy to reduce the time frame from pathogen identification to the development and emergency approval for human use of a reasonably safe and effective priority countermeasure against a novel or unknown pathogen or toxin. Requires the report to include: (1) technical impediments to reducing this time frame; (2) research, development, and technology needs to address these impediments; and (3) potential liability concerns stemming from distribution of rapidly-developed priority countermeasures. Allows the Secretary to contract with any firm or institution to conduct necessary research and analysis for this report. Requires the Secretary of Health and Human Services (HHS) to establish a system to rapidly: (1) establish clinical research programs to examine the safety and efficacy of treatments for novel, unknown, or bioengineered pathogens or toxins; and (2) disseminate results and recommendations to clinicians. Authorizes establishment of a fund to support such clinical research. Requires the Secretary of Homeland Security to establish an interagency working group to carry out this Act. Amends the Public Health Service Act to require the Secretary of HHS to conduct research to rapidly identify, develop, produce, and approve for human use priority countermeasures. Requires the Secretaries of Defense and HHS to carry out research, development, and procurement to provide the federal government with the capability to rapidly identify, develop, produce, and approve for human use under emergency conditions priority countermeasures against a novel, unknown, or engineered pathogen or toxin for which no existing countermeasure has been determined to be safe or efficacious.

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

Timeline

  1. 29 July 2005

    Introduced

    Referred to the Committee on Energy and Commerce, and in addition to the Committees on Armed Services, and Homeland Security, for a period to be subsequently determined by the Speaker, in each case for consideration of such provisions as fall within the jurisdiction of the committee concerned.

    Source: IntroReferral

  2. 29 July 2005

    Introduced

    Referred to the Committee on Energy and Commerce, and in addition to the Committees on Armed Services, and Homeland Security, for a period to be subsequently determined by the Speaker, in each case for consideration of such provisions as fall within the jurisdiction of the committee concerned.

    Source: IntroReferral

  3. 29 July 2005

    Introduced

    Sponsor introductory remarks on measure. (CR E1712)

    Source: IntroReferral

  4. 29 July 2005

    Introduced

    Introduced in House

    Source: IntroReferral

  5. 29 July 2005

    Introduced

    Introduced in House

    Source: IntroReferral

  6. 5 August 2005

    Referred

    Referred to the Subcommittee on Health.

    Source: Committee

  7. 22 August 2005

    Referred

    Referred to the Subcommittee on Emergency Preparedness, Science, and Technology.

    Source: Committee

  8. 19 September 2005

    Referred

    Referred to the Subcommittee on Terrorism, Unconventional Threats and Capabilities.

    Source: Committee

Votes

No vote records are attached yet.

Versions

Documents

3 official files

Introduced in House (text)

View fileDownload file

Sponsors

Related records

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Sources

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