S.613 - A bill to prohibit the use of Federal funds to approve certain biologics license applications by the Food and Drug Administration.

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U.S. Congress - Text of S.613 as Introduced in Senate A bill to prohibit the use of Federal funds to approve certain biologics license applic...A non-profit, non-partisan public resource
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S 613 ISCommentsClose CommentsPermalink
111th CONGRESSCommentsClose CommentsPermalink
1st SessionCommentsClose CommentsPermalink
S. 613CommentsClose CommentsPermalink
To prohibit the use of Federal funds to approve certain biologics license applications by the Food and Drug Administration.CommentsClose CommentsPermalink
IN THE SENATE OF THE UNITED STATESCommentsClose CommentsPermalink
March 17, 2009CommentsClose CommentsPermalink
Mr. BROWNBACK introduced the following bill; which was read twice and referred to the Committee on Health, Education, Labor, and PensionsCommentsClose CommentsPermalink
A BILLCommentsClose CommentsPermalink
To prohibit the use of Federal funds to approve certain biologics license applications by the Food and Drug Administration.CommentsClose CommentsPermalink
Be it enacted by the Senate and House of Representatives of the United States of America in Congress assembled,CommentsClose CommentsPermalink
Notwithstanding any other provision of law, no funds provided by any Appropriations Act enacted before the date of enactment of this Act that remain unobligated as of such date of enactment shall be used by the Food and Drug Administration to process a biologics license application under section 351 of the Public Health Service Act (
(1) information submitted in such application, or any other information available to the Secretary of Health and Human Services, shows that the biologic product is, bears, or contains a listed select agent or toxin within the meaning of part 331 of title 7, Code of Federal Regulations, part 121 of title 9, Code of Federal Regulations, and part 73 of title 42, Code of Federal Regulations; andCommentsClose CommentsPermalink
(2) the entity filing such application has, during the 2-year period before the date of submission of such application to the Secretary--CommentsClose CommentsPermalink
(A) marketed, sold, or distributed that product in the Islamic Republic of Iran;CommentsClose CommentsPermalink
(B) provided select agents or toxins to institutions in the Islamic Republic of Iran, including to the Pasteur Institute in Tehran and Tehran University;CommentsClose CommentsPermalink
(C) submitted patient safety or efficacy data produced through experiments or trials that would violate the laws of the United States governing the proper handling of select agents or toxins; orCommentsClose CommentsPermalink
(D) been the subject of an investigation by the Office of Foreign Assets Control of the Department of Treasury, the Bureau of Industry and Security of the Department of Commerce, or the Department of Justice for potential violations of the Iran Sanctions Act of 1996 (
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