MDUFMA II under scrutiny, post-market fees considered

05/24/2007 | Medical Devices Today

This analysis of the proposed Medical Device User Fee & Modernization Act looks at areas in the bill that deal with speeding up the premarket review process, funding, third-party issues and patient safety. One member of the House subcommittee charged with overseeing reauthorization of the user fee has suggested that some of the money be allotted for post-market surveillance to enhance safety.

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