Bipartisanship Brings About Needed Reforms to FDA
Washington,
May 10, 2012
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Maggie Seidel
((202) 225-3861)
Congressman Morgan Griffith (R-VA) issued the following statement today after joining his colleagues to unanimously pass the Food and Drug Administration (FDA) Reform Act of 2012: Congressman Griffith was also pleased to have a chance to vote on The Creating Hope Act (CHA), which is included in the FDA Reform Act. Earlier this year, Congressman Griffith met with Brianna Commerford, a key advocate for this legislation. At just nine years old, Brianna was diagnosed with stage IV Hodgkin's lymphoma, a cancer in the lymph nodes. After about a year of chemotherapy, eight surgeries, and a deeply committed spirit, she beat this horrible cancer and has now been in remission for more than three years. The FDA’s review process is often very lengthy. If, however, a drug or biologics company develops a new treatment for particular diseases, like blinding trachoma or new forms of tuberculosis, they qualify for the FDA’s priority review voucher program. The CHA, a bipartisan bill, would expand the FDA’s priority review voucher program to allow pharmaceutical companies to expedite FDA review of more profitable drugs or biologics in return for developing treatments for rare pediatric diseases. Click here to read a legislative summary of the FDA Reform Act of 2012.
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