I thank the gentleman from New Jersey. Mr. Speaker, I rise in strong support of H.R. 5651, to reauthorize the prescription drug and medical device user-fee programs, to establish new user-fee programs for generic drugs and biosimilars, and also to give substantial new authorities to the Food and Drug Administration, with the support of the industry, to provide broad additional protections to American consumers. H.R. 5651 is an excellent example of the great good that can be done when both parties come together in the spirit of bipartisanship, cooperation, and compromise, and when they work with consumers and the industry to achieve a bill supported by all. This legislation will ensure the timely access to safe and effective drugs and medical devices, encourage the development of the innovative drug treatments for our children, and improve the Food and Drug Administration's current authority to deal with drug shortages. More importantly, this legislation will provide FDA with much-needed new authorities to secure the safety of our drug supply and to help prevent another incident like that unfortunate one involving heparin, in which over 80 people died from a blood thinner which was contaminated from where it came, in China, and which also sickened over 100 people of whom we know. H.R. 5651's drug supply chain provisions will improve information FDA has about domestic and foreign drug manufacturers.…
On the recordMay 30, 2012
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I have no further requests for time, I strongly urge my colleagues to support this legislation, and I yield back the balance of my time.
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