Analysis of US FDA Data Shows 37% Increase in 510(k) Clearance Times Since 2006An examination of publicly available FDA data by Emergo Group on 510(k) clearances over the last five years indicates that 80% of devices receive clearance within six months.
AUSTIN, TX, June 23, 2011 /24-7PressRelease/ -- Emergo Group, an Austin-based consulting firm that assists medical device manufacturers with regulatory compliance, has completed a comprehensive analysis of medical device
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