I thank the chairman for yielding me the time. It is significant today to be here and be supporting H.R. 2430, the Food and Drug Administration Reauthorization Act of 2017. The passage of this bill provides certainly the security to the scientists who are working even now in pursuit of better cures and, of course, hope for patients across the country who are awaiting better treatments of the diseases that are afflicting them. By reauthorizing the Food and Drug Administration user fee program, we are ensuring that the Food and Drug Administration can continue to officially operate and approve new drugs for the market. Upon becoming chairman of the Subcommittee on Health this year, I had the privilege of convening four separate legislative hearings on the policies that are included in H.R. 2430. In each of those hearings, we heard about the tremendous success of the user fee programs in expanding access to affordable medications, supporting biomedical innovation, and maintaining high standards at the FDA for safety, efficacy, and quality. H.R. 2430 will build upon these successes and will also build upon the achievements that we achieved in the last Congress, in the 21st Century Cures Act. And now we can ensure that the FDA has resources necessary to get medical treatments and cures to patients and healthcare providers as quickly as possible.…
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By direction of the Committee on Rules, I call up House Resolution 1341 and ask for its immediate consideration. The Clerk read the resolution, as follows: H. Res. 1341 Resolved, That upon adoption of this resolution it shall be in order…
I thank the gentlewoman for yielding. Mr. Speaker, the reason we are here is because the average family of four is paying over $17,000 more per year thanks to the policies of the Biden-Harris administration and their allies in Congress. In…
May I inquire as to how much time I have remaining. The SPEAKER pro tempore. The gentleman from Texas has 14 minutes remaining.
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