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 Hch 551 Form 2011

2011-2025 Form

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foreign ee will come to order the chair recognizes himself for five minutes for an opening statement the prescription drug user fee Act padufa was first authorized by Congress in 1992 with the goal of Expediting human drug applications through the Food and Drug administration's approval process under the act and its subsequent reauthorization the drug industry pays user fees to FDA and FDA commits to meet performance goals such as reviewing applications within a certain period of time this construct was designed to give industry certainty and predictability but also to speed new drugs and treatments to the public details of the agreement between FDA and Industry will be published on September 1st of this year and by January 15 2012 FDA will send its final recommendations to Congress the current padufa authorization expires September 30 2012. and it is my intention to have the reauthorization legislation signed into law by June 30 of next year badufa is too important to leave to

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