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FDA Advisors Declare 'FDA Science and Mission at Risk'
Date:1/29/2008

' situation that has to change."

---Michael Taylor, former FDA & USDA official; Research Professor, The George Washington University

"FDA is trying to transition from a heavily paper/manual system to an all electronic system that is reliable, secure, and can analyze data on new and existing products to quickly recognize safety issues. All the centers need to work on the same IT platform, one capable of handling the volume and complexity of data submitted. None of this can be achieved until the FDA has enough appropriated money dedicated to a technology overhaul and maintenance. Notably, the Subcommittee report identifies IT deficiencies as one of its three major findings."

--Phyllis Greenberger, President and CEO, Society for Women's Health Research


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SOURCE Alliance for a Stronger FDA
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