Guthrie Involved in House-Passed Bill to Modernize Health Care System, Spark Innovation in Medical Cures
Washington, DC,
July 10, 2015
Tags:
Health Care
21st Century Cures has been a longtime coming, but I'm excited about what our committee has put together. From Alzheimer's to ALS, this bill will have a real impact on the many Americans suffering from these debilitating diseases, said Congressman Guthrie.
Washington, DC – Today, Congressman Brett Guthrie (KY-02) voted in support of H.R. 6, the 21st Century Cures Act. The landmark, bipartisan legislation will help deliver more cures, treatments and therapies to patients. “Today’s innovation is tomorrow’s cures,” said Congressman Guthrie, Vice Chairman of the Energy and Commerce Committee’s Health Subcommittee. “21st Century Cures has been a longtime coming, but I’m excited about what our committee has put together. From Alzheimer’s to ALS, this bill will have a real impact on the many Americans suffering from these debilitating diseases.” The 21st Century Cures Act will unlock innovation in a number of ways: by removing barriers to increased research collaboration; incorporating the patient perspective into the drug development and regulatory review process; modernizing clinical trials, providing new incentives for the development of drugs that treat rare diseases; investing in 21st Century science; and helping to keep and create jobs here at home. H.R. 6 is the product of more than one year of listening to patients and medical experts about what steps Congress can take to help researchers, caregivers and innovators unleash the power of 21st Century science and technology. H.R. 6 was unanimously passed out of committee in May (51-0) and passed in the House today by a margin of 344-77. As an original cosponsor of the legislation, some provisions championed by Congressman Guthrie are included in the final bill. Among those items are provisions authorizing grants for the study of continuous manufacturing of drugs and biologics, and requiring guidance to be issued by the Food and Drug Administration (FDA) that clarifies the process for approval of point-of-care diagnostic tests. ### |