July 2007
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July 2007
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House
Passes MDUFMA Reauthorization
On July 12, the U.S. House of Representatives passed omnibus FDA legislation, including the reauthorization of the Medical Device User Fee and Modernization Act. The bill mirrors the Senate version, which sets device user fee rates for the next five fiscal years and establishes a new device facility registration fee. The House version did not include controversial language which would have superseded court precedent relative to FDA preemption in products liability cases. A House-Senate Conference is expected to review the legislation for final
passage.
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