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The manufacturer of a Part B rebatable drug may submit a Suggestion of Error about the information in their Preliminary Rebate Report and the report detailing the preliminary reconciliation of the rebate amount to CMS, for its discretionary consideration, if the manufacturer believes that there is a mathematical error or errors to be corrected before the Rebate Report or a subsequent reconciliation of the rebate amount, as applicable, is finalized

This is a decrease of 4 percentage points from the currently approved estimate of 14 percent in the ( CY 2024 PFS final rule (88 FR 79443)

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This is similar to those used in a urine drug test