21st Century Cures legislation approved in the House Energy & Commerce Health Subcommittee fleshes out provisions intended to reduce the number of FDA premarket submissions from device companies, including a measure allowing third-party quality systems certifications to replace certain premarket submissions and a provision pressing FDA to identify more devices that could be exempted from the 510(k) process.
The subcommittee approved the latest Cures draft in a voice vote at a May 14 markup, sending it...
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