The Food & Drug Administration is changing the way its advisory panels deliberate and vote on medical devices under review at the federal watchdog.
The Food & Drug Administration is making changes to the way its advisory panels deliberate over and vote on medical devices under review by the federal watchdog agency.
As of May 1, the FDA is instituting new procedures for the panels, groups of experts assembled to review and discuss data and information on devices undergoing pre-market review.
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