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Food and Drug Administrations pre-marketing approval

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In aggregate, when combined with our currently approved per response time estimate, the decrease in 3,300 respondents who will submit data for the MVP quality performance category will result in a change of 8,766 hours and $1,066,714 for the eCQM collection type, 4,877 hours and $585,225 for the CQM and QCDR collection type, and 7,826 hours and $912,928 for the Medicare Part B claims collection type

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[207] The observational data presented in the review suggests a link between oral health and mortality in patients on RRT