US Congress House Bill 3932 (Prior Session Legislation)

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Spectrum: Partisan Bill (Republican 8-0)
Status: Introduced on October 27 2009 - 25% progression, died in committee
Action: 2009-10-28 - Referred to the Subcommittee on Health.
Pending: House Subcommittee on Health Committee
Text: Latest bill text (Introduced) [PDF]

Strengthening of FDA Integrity Act of 2009 - Amends the Federal Food, Drug, and Cosmetic Act to apply debarment provisions currently applicable to abbreviated new drugs to any drug products, including new drugs, animal drugs, exported drugs, biological products, and medical devices. Expands the conditions under which persons (i.e., partnerships, corporations, and associations) are subject to mandatory and permissive debarment preventing such persons from submitting an application for approval of a drug product. Requires the Secretary of Health and Human Services (HHS), in determining the appropriateness and the period of debarment, to consider whether debarment will affect the public health because sufficient quantities of the drug would not be available. Requires the Secretary to annually report to Congress on the implementation of debarment provisions.

Strengthening of FDA Integrity Act of 2009

Rep. Joe Barton [R-TX]	Sen. Marsha Blackburn [R-TN]	Rep. Mary Bono Mack [R-CA]	Rep. Michael Burgess [R-TX]
Rep. John Shimkus [R-IL]	Rep. John Sullivan [R-OK]	Rep. Lee Terry [R-NE]	Rep. Greg Walden [R-OR]

Date	Chamber	Action
2009-10-28		Referred to the Subcommittee on Health.
2009-10-27		Referred to the House Committee on Energy and Commerce.

Type	Source
Summary	https://www.congress.gov/bill/111th-congress/house-bill/3932/all-info
Text	https://www.congress.gov/111/bills/hr3932/BILLS-111hr3932ih.pdf