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FDA Changes Process for Medical Device Advisory Committees
April 26, 2010
WASHINGTON, April 26 -- The U.S. Department of Health and Human Services' Food and Drug Administration issued the following news release:

The U.S. Food and Drug Administration today announced that it will change the way its expert panels review and discuss data and information during public hearings on medical devices under review for premarket approval, effective May 1, 2010.

The changes were prompted by an increasing number of medical device advisory panel meeting . . .

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