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United States · Bill · HR

H.R. 2090 (109th)

Food and Drug Administration Improvement Act of 2005

openUnited States· United States Congress· EN

Introduced

4 May 2005

Last action

21 June 2006 · Introduced

Status

Sponsor introductory remarks on measure. (CR H4358-4359)

Sponsors

Rep. Hinchey, Maurice D. [D-NY-22], Rosa DeLauro, Rep. Stupak, Bart [D-MI-1], Raúl Grijalva, Rep. Woolsey, Lynn C. [D-CA-6], Ed Case, Rep. Lynch, Stephen F. [D-MA-8], Rep. Evans, Lane [D-IL-17], Rep. Fattah, Chaka [D-PA-2], Rep. McNulty, Michael R. [D-NY-23], Sen. Sanders, Bernard [I-VT], Rep. Wexler, Robert [D-FL-19], JOHN CONYERS, Rep. Kucinich, Dennis J. [D-OH-10], James McGovern, Rep. Jackson, Jesse L., Jr. [D-IL-2]

Subjects

Healthcare

Source updated

15 August 2025

Healthcare

Summary

Food and Drug Administration Improvement Act of 2005 - Amends the Federal Food, Drug, and Cosmetic Act (FFDCA) to require that all fees collected for the review of applications for human drugs, devices, and animal drugs be deposited in the general fund of the Treasury. Makes available amounts necessary for the Secretary of Health and Human Services to review such applications. Prohibits the Secretary from entering into agreements with persons from whom such fees are collected and terminates any existing agreements. Requires the Secretary to: (1) establish the Center for Postmarket Drug Safety and Effectiveness within the Food and Drug Administration (FDA) to regulate approved drugs; and (2) transfer to the Center all responsibilities for such regulation from the Center for Drug Evaluation and Research and the Center for Biologics Evaluation and Research. Allows the Secretary to require manufacturers of approved drugs to conduct studies of an identified significant safety issue with the drug. Deems a drug to be misbranded if it does not meet the Secretary's requirements, including requirements for labeling and conducting postmarket studies. Requires the Secretary to follow the interpretation that the FDA used in 1999 that the FFDCA and Public Health Service Act establish minimal standards but do not preclude additional state requirements. Requires the Secretary to cease intervening in product liability civil actions to argue another interpretation. Sets forth procedures for advisory committee meetings to ensure that the committee is fairly balanced. Prohibits any exemptions from being granted to advisory committee members from rules prohibiting members from having a personal financial interest in the outcome. Requires doctors to inform patients and obtain consent to prescribe an approved drug for a purpose that has not been approved by the FDA.

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

Timeline

  1. 4 May 2005

    Introduced

    Referred to the House Committee on Energy and Commerce.

    Source: IntroReferral

  2. 4 May 2005

    Introduced

    Introduced in House

    Source: IntroReferral

  3. 4 May 2005

    Introduced

    Introduced in House

    Source: IntroReferral

  4. 23 May 2005

    Referred

    Referred to the Subcommittee on Health.

    Source: Committee

  5. 21 June 2006

    Introduced

    Sponsor introductory remarks on measure. (CR H4358-4359)

    Source: IntroReferral

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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