H.R.6378 - Strengthening of FDA Integrity Act of 2008110th Congress (2007-2008)
|Sponsor:||Rep. Barton, Joe [R-TX-6] (Introduced 06/26/2008)|
|Committees:||House - Energy and Commerce|
|Latest Action:||House - 06/26/2008 Referred to the Subcommittee on Health. (All Actions)|
This bill has the status Introduced
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Summary: H.R.6378 — 110th Congress (2007-2008)All Information (Except Text)
Introduced in House (06/26/2008)
Strengthening of FDA Integrity Act of 2008 - 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 to initiate debarment not later than one year after a person or individual is convicted of a felony.
Requires the Secretary, 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.