Specialists in providing claim administration audits.
The primary objective of our PBM Audit approach is to identify errors and/or problems in the administration of the plan — for immediate corrective action, or possible reimbursement. Additionally, our findings will verify contract adherence, identify problem causes, and provide recommended actions for future savings.
Compared to other types of health plan audits, the existence of a uniform data set and established protocols for PBM's to adjust for errors make recoveries in this area more tenable. It is not unusual in our experience with initial audits for 1%-3% of paid claims to be identified as potentially recoverable. Because each audit is unique with respect to PBM and plan specifications, no assurances are made or implied here as to what level of recoverable dollars may be identified or achievable. However, the following chart provides a breakdown of the types of recoverable errors typically seen:
Important Differences in Rx Claim Processing Prescription drug claims differ from medical claims significantly in the ways they are incurred and processed. In addition to (or as a result of) the "content" of prescription claims, the claims paying process places much higher reliance on electronic data. And, as noted above, there exists a uniform data set used by all parties. Accordingly, protocols for identifying and crediting overpayments to plan sponsors by PBM's therefore are established and accepted as common practice to a much greater degree than with medical claims audits.
Our approach employs electronic review and analysis of pharmacy benefit claims data using highly automated, proprietary audit systems. Because the systems were originally developed for very high volume processors, the depth and breadth of review is extremely thorough. The following table lists general categories of errors that the system is capable of detecting:
Your pharmacy plan specifications will be loaded into the system and 100% of the claims paid during the specified audit period will be electronically "reprocessed" and subject to electronic review and verification. Claims flagged for failing this verification will be detailed in line-item report format along with a narrative explanation of the discrepancy and the corresponding paid claims dollar overcharge. Through substantive testing and review with the PBM, this information will be verified and the final discrepant claims total will be utilized to determine the total recovery potential for the period of review.
The PBM's performance also will be evaluated in such areas as dispensing accuracy, financial accuracy, generic substitution efficiency rate, clinical management programs, savings guarantees (retail pharmacy discounts, mail order discounts), rebate guarantees, product switch/intervention efforts, lower of UCR price guarantee, electronic edit and concurrent DUR savings, retrospective DUR savings. Additionally, our findings will verify contract adherence, identify problem causes, and provide recommended actions for future savings.
Our drug pricing and discount analysis will compare the price basis per unit charged for the NDC (National Drug Code) adjudicated on the dispensing date with national drug price data sources in effect on that date. Any differences in price basis and discount level will be noted and detailed on a per claim basis. Generic discount verification will be conducted in the same manner. This pricing will be compared to the original claims and each difference will be documented.
Our final report will include a detailed summary of findings by category. Amounts of overcharge per claim will be provided for each category on a per-claim basis, and a narrative of category findings and recommendations will be included noting findings of significance as well as recommendations for future corrective action.This will constitute the basis for requesting reimbursement of overpayments from the PBM.
We will review our report and recommendations with you. If adjustments to the reports are warranted, they will be made and the adjusted output will be provided. Corrective action recommendations and recovery from this point forward can then be undertaken with or without our involvement.
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