122436 O5 - Attachment C1 - Confirmations & Questionnaire.xlsx

XLSX spreadsheet 49 KB Posted

Attached to
Administrative Support Services for the State of Nebraska Employee Health Care Prescription Drug Benefit Plans
Solicitation number
122436 O5
Issued by
Blaine County, Nebraska

About this file

This document is a Confirmations & Questionnaire attachment (Attachment C1) for RFP #122436 O5, issued by the State of Nebraska for Administrative Support Services for the state's employee health care prescription drug benefit plans. The solicitation seeks a Pharmacy Benefit Manager (PBM) to provide comprehensive administrative services for approximately 13,600 enrolled members, including active employees, pre-65 retirees, COBRA participants, and their dependents. The RFP was released on June 9, 2025, with proposal responses due by July 18, 2025, and an anticipated contract award in October 2025. The initial contract term will run through June 30, 2029, with options to renew for two additional one-year periods, with the benefit plan year commencing on July 1, 2026.

The procurement focuses on a self-funded PBM administrator with transparent pricing models, including guaranteed minimum AWP discounts for brand and generic medications, and comprehensive rebate guarantees. The cost structure includes per member per month (PMPM) administrative fees, with an estimated consistent enrollment of around 28,386 members throughout the contract period. Evaluation criteria include 25 points for Corporate Overview, 55 points for Technical Response, and 20 points for Cost, with potential additional points for vendor demonstrations. The state requires a dedicated Account Management Team, HIPAA compliance, and performance guarantees with potential financial penalties ranging from $2,000 to $50,000 per occurrence, emphasizing a rigorous and performance-driven procurement process.

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Other files

File Type Posted
Intent to Award.pdf PDF
122436 O5 - Optum Response.pdf PDF
122436 O5 - Attachment A - Intent to Propose.docx DOCX document
122436 O5 - Addendum One- Questions & Answers and Updated Attachment C.docx DOCX document
122436 O5 - BCBS Response_.pdf PDF
122436 O5 - BCBS Response.pdf PDF
PBM 122436 O5- Addendum Two- Questions and Answers- Round Two V2.pdf PDF
122436 O5 Prescription Drug Benefits Plan RFP.pdf PDF
122436 O5 - PBM Evaluation Criteria.docx DOCX document
122436 O5 - Rightway Response.pdf PDF
122436 O5 - Attachment C1 - Confirmations & Questionnaire.xlsx XLSX spreadsheet
122436 O5 Prescription Drug Benefits Plan RFP.docx DOCX document
122436 O5 - Cost Sheet.xlsx XLSX spreadsheet
FinalEvaluationDocument.pdf PDF
122436 O5 UnitedHealthcare Response.pdf PDF
122436 O5 - Attachment D - Performance Guarantees.xlsx XLSX spreadsheet
122436 O5 - Attachment B - Business Associate Agreement.doc DOC document
122436 O5 Solicitation List of Respondents.pdf PDF
122436 O5 - MedImpact Response.pdf PDF
122436 O5 Prescription Drug Benefits Plan RFP.docx DOCX document
122436 O5 - Attachment D - Performance Guarantees.xlsx XLSX spreadsheet
122436 O5 - Attachment C1 - Confirmations & Questionnaire.xlsx XLSX spreadsheet
122436 O5 - Attachment B - Business Associate Agreement.doc DOC document
122436 O5 - Attachment A - Intent to Propose.docx DOCX document
122436 O5 - Cost Sheet.xlsx XLSX spreadsheet
122436 O5 - Addendum One- Questions & Answers and Updated Attachment C.docx DOCX document
122436 O5 Solicitation List of Respondents.pdf PDF
122436 O5 Prescription Drug Benefits Plan RFP.pdf PDF
122436 O5 - PBM Evaluation Criteria.docx DOCX document
PBM 122436 O5- Addendum Two- Questions and Answers- Round Two V2.pdf PDF
122436 O5 - PBM Evaluation Criteria.docx DOCX document
122436 O5 - Cost Sheet.xlsx XLSX spreadsheet
122436 O5 - Attachment A - Intent to Propose.docx DOCX document
122436 O5 - Addendum One- Questions & Answers and Updated Attachment C.docx DOCX document
122436 O5 - Attachment B - Business Associate Agreement.doc DOC document
122436 O5 - Attachment D - Performance Guarantees.xlsx XLSX spreadsheet
122436 O5 Prescription Drug Benefits Plan RFP.pdf PDF
122436 O5 Prescription Drug Benefits Plan RFP.docx DOCX document
PBM 122436 O5- Addendum Two- Questions and Answers- Round Two V2.pdf PDF
122436 O5 - Attachment B - Business Associate Agreement.doc DOC document
122436 O5 - Addendum One- Questions & Answers and Updated Attachment C.docx DOCX document
122436 O5 - Attachment C1 - Confirmations & Questionnaire.xlsx XLSX spreadsheet
122436 O5 - PBM Evaluation Criteria.docx DOCX document
122436 O5 Prescription Drug Benefits Plan RFP.docx DOCX document
122436 O5 - Cost Sheet.xlsx XLSX spreadsheet
122436 O5 - Attachment D - Performance Guarantees.xlsx XLSX spreadsheet
122436 O5 Prescription Drug Benefits Plan RFP.pdf PDF
122436 O5 - Attachment A - Intent to Propose.docx DOCX document
122436 O5 - Attachment A - Intent to Propose.docx DOCX document
122436 O5 Prescription Drug Benefits Plan RFP.pdf PDF
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Instructions

ATTACHMENT C - CONFIRMATIONS & QUESTIONNAIREBidder:NAME
SOLICITATION NUMBER - 122436 O5
Instructions for Completing this Questionnaire Workbook
• Provide succinct yet informative responses.
• Bidder should complete all questions in this Questionnaire.

Confirmations

ATTACHMENT C - CONFIRMATIONS & QUESTIONNAIREBidder:
SOLICITATION NUMBER - 122436 O5NAME
All Bidders must comply with the following conditions regarding the RFP. Confirm your capability to meet each of the following with a response of Confirmed or Not Confirmed. If your response varies by the plan option(s) you are quoting, please explain. If a Bidder takes exception to any of these confirmations, it must be clearly noted. These confirmations will also explicitly apply to any subcontractors used.
ConfirmationsVendor Response
A.GENERALResponse (Confirmed/Not Confirmed)
A.1PBM agrees the State has the right to terminate the contract for any reason without penalty of any kind upon ninety (90) days-notice. The State will receive all rebates accrued during the tenure of the contract.
A.2PBM agrees the State reserves the right to audit the State’s PBM claim records, and any other financial records as they pertain to the pharmacy benefit program, whenever the State deems it appropriate, using whatever methodology and vendor they choose. Such claim audits may be performed by the State’s personnel or by outside auditors selected by the State.
A.3PBM agrees if selected as a finalist, to provide a signature ready contract and that your responses to the RFP, including all attachments, will be included as an attachment to the contract. The State reserves the right to negotiate additional changes to the final contract.
A.4PBM agrees it shall provide a fully pass-through network, meaning it will bill the State the same as it reimburses network pharmacies for retail, mail order, and specialty drug claims. The PBM shall also pass-through 100% of Rebates to the State. All business practices, processes, and sources of revenue must be fully disclosed upon request.
A.5PBM agrees the State reserves the right to carve-out specialty and mail order drug fulfillment and/or utilization management if it determines it is financially advantageous to do so.
A.6PBM agrees to develop a member satisfaction survey approved by the State to be sent to each plan member, conduct the survey, and collect and report respondent results on an annual basis at no additional cost to the State.
A.7PBM agrees to provide easy-to-access management reports approved by the State in Excel or in a format that can be exported to Excel at least quarterly and as otherwise requested by the State.
A.8PBM agrees to abide by all Federal and State laws and requirements throughout the contract term.
A.9PBM will not render or administer services off-shore, and all work performed will be in the contiguous United States.
B.CONTRACT DEFINITIONSResponse (Confirmed/Not Confirmed)
B.1Contract Definitions
a. AWP (Average Wholesale Price) –The actual reported "AWP" from Medi-Span for the specific NDC-11 on the Day of Service for all channels (i.e., Retail, Mail, and Specialty). Claims will not use an average AWP or pre-settlement AWP, nor will the AWP be externally calculated, altered, or adjusted. Claims at Mail and Specialty pharmacies will use the AWP of the actual package size and NDC-11 used to dispense (not the package size of the prescription dispensed or alternative package sizes).
b. Brand Drug - For adjudication purposes, a drug that is approved by the U.S. Food and Drug Administration (FDA) and is distributed under an FDA Application Type of new drug application (NDA) or biologic license application (BLA), and which is not an Authorized Generic and which is not a House Generic. In instances where the Brand or Generic status of a drug, as determined by the Contractor relying on an independent published source, differs from this definition, the Contractor may rely on its standard drug classification system for operational purposes of claim adjudication. All Brand Pricing Guarantees will be reconciled based on Medi-Span multi-source code field M, N, or O, excluding House Generics, as defined herein, and shall mean drugs or devices for which the Medi-Span Multisource Code field contains “M” (co-branded product), or “N” (single source brand), or “O” (originator). If the multi-source code in Medi-Span is "O", and there is a DAW code of 3, 4, 5, 6, or 9, the drug shall be considered a generic.
c. Biosimilar - A FDA-approved type of biological product that is highly similar to and has no clinically meaningful differences in terms of safety and effectiveness from its respective FDA-approved biological reference product, under Section 351(k) of the Public Health Service Act, as added by the Biologics Price Competition and Innovation Act of 2009.
d. Claim - Prescription drugs, over the counter (OTC) products, drug products, medical supplies, or medical devices that are processed and paid through PBM's adjudication system or otherwise transmitted/processed by the PBM in accordance with State's applicable benefit plan design. Bidder agrees its financial bid is based on approved and Paid Claims only and will exclude all rejected, withdrawn, denied and/or reversed Claims.
e. Compound Drug - A medication that requires compounding by pharmacists because it is not available from a pharmaceutical manufacturer in the prescribed form or strength. Compound drugs consist of two or more solids, semi-solids, or liquids where at least one of which is a Covered Product.
f. Covered Product – The prescription drugs, supplies, and other items that are covered under the Benefit or treated as covered pursuant to a coverage determination appeal.
g. Generic Drug - For adjudication purposes, a drug that is approved by the U.S. Food and Drug Administration (FDA) and is distributed under an FDA Application Type of abbreviated new drug application (ANDA), or which is an Authorized Generic or which is processed as a House Generic. In instances where the Brand or Generic status of a drug, as determined by the Contractor relying on an independent published source, differs from this definition, the Contractor may rely on its standard drug classification system for operational purposes such as claim adjudication. All Generic Pricing Guarantees will be reconciled based Medi-Span multi-source code filed of Y or House Generic, as defined herein.
h. Authorized Generic Drug - Any drug sold, licensed, or marketed under a new drug application (NDA) approved by the Food and Drug Administration (FDA) under section 505(c) of the Federal Food, Drug, and Cosmetic Act (FFDCA) that is marketed, sold or distributed under a different labeler code, product code, trade name, trademark, or packaging (other than repackaging the listed drug for use in institutions) than the Brand Drug.
i. House Generic Drug - A drug with the multi-source code field in Medi-Span of O when there is a DAW code of 5.
j. Ingredient Cost - The total cost for a Covered Product on a Paid Claim, excluding Administrative Fees, Copay, Dispensing Fees, POS Rebates, government-imposed service fees, and taxes, in accordance with the terms of the Plan.
k. MAC – maximum allowable cost.
l. Rebates – Compensation or remuneration of any kind received or recovered from a pharmaceutical manufacturer or rebate aggregator attributable to the purchase or utilization of covered drugs by eligible persons, including, but not limited to, incentive rebates categorized as mail order purchase discounts; credits; rebates, regardless of how categorized; market share incentives; promotional allowances; commissions; educational grants; market share of utilization; drug pull-through programs; implementation allowances; clinical detailing; rebate submission fees; and administrative or management fees. Rebates also include any fees that PBM receives from a pharmaceutical manufacturer for administrative costs, formulary placement, and/or access.
m. Manufacturer Administrative Fees - Those fees received by PBM or PBM's Affiliate(s) from pharmaceutical manufacturers or intermediaries pursuant to a contract between PBM or PBM's Affiliate(s) and a drug manufacturer to manage placement of Covered Products on PBM's Formulary and administering, invoicing, allocating and collecting Rebates that are attributable to Covered Products dispensed to Members.
n. Formulary – The list of clinically appropriate Covered Products covered by the State, organized into different tiers or levels indicating potential member cost share for each Covered Product.
o. Copay – The portion of the charge for each Covered Product dispensed to a Member that is the responsibility of such enrollee (e.g., copayment, coinsurance, cost sharing, and/or deductibles under initial coverage limits and up to annual out-of-pocket thresholds) as provided under the Benefit.
p. Paid Claims – Defined as all transactions made on eligible members that result in a payment to pharmacies or members from the State or State member copays. (Does not include reversals and adjustments.) Each unique prescription that results in payment shall be calculated separately as a paid claim.
q. Member – All eligible employees and their eligible dependents enrolled under the State prescription benefit program.
r. Market Check – An evaluation of prescription drug pricing based on benchmarks derived from existing market PBM agreements of comparable plans.
s. 340B Claim - A Claim identified by the submission of "20" in the Submission Classification Code field 420-DK and/or a Claim submitted by a pharmacy owned by a covered entity, as defined in Section 340B(a)(4) of the Public Health Services Act, whose 340B status is coded as "39" in the NCPDP DataQ database. Claims incurred at a PBM owned, operated, or affiliated mail or specialty pharmacy are not included in this definition.
t. GCN – A five-character numeric figure that represents the clinical formulation; it is specific to active ingredient list, route of administration, dosage form, and drug strength.
u. GPI or GP14 - Generic Product Identifier reported by Medi-Span. It is a 14-character hierarchical classification that identifies drugs from their primary therapeutic use down to the unique interchangeable product regardless of manufacturer or package size.
v. U&C Price (Usual and Customary) – The actual retail price charged by a Participating Pharmacy for a specified drug if purchased in a cash transaction on the date the drug is dispensed, as reported to Supplier by the Participating Pharmacy.
w. ZBD Claim (Zero Balance Due) – Any claim for which the Member is response under the applicable Benefit Plan for the full amount of the Claim's Gross Drug Cost and State is responsible for no portion of the Claim's Gross Drug Cost.
B.2Minimum Brand and Minimum Generic Discount Guarantees for both mail and retail shall be defined as follows: (1 – Aggregate Ingredient Cost/Aggregate AWP)
a. Aggregate Discounted Ingredient Cost prior to application of plan specific copayments will be the basis of the calculation.
b. Aggregate AWP will be sourced from Medi-Span.
c. Dispensing Fees are not included in the Aggregate Ingredient Cost.
d. Zero Balance Due claims will be included in the guaranteed measurement for AWP, ingredient cost, achieved discounts or dispensing fee calculations at the discounted cost before copay.
e. All guarantee measurements shall be calculated prior to the Copay being applied. Entire dollar-for-dollar shortfalls, prior to the application of Copay, will be reimbursed to the State without any adjustments to remove zero balance due or excess copayment claims.
f. Both the Aggregate Ingredient Cost and Aggregate AWP from the actual date of claim adjudication will be used.
g. Aggregate AWP will be the date sensitive, 11-digit NDC of the actual product dispensed at both retail and mail and specialty.
h. Non-MAC, MAC, single-source, and multiple source generic products are to be included in the generic guarantee measurement (regardless of the exclusivity period and/or number of manufacturers) and excluded from brand guarantee measurement.
i. Compounds, OTC claims, and claims with ancillary charges will be excluded from the guarantee measurements for retail and mail order components.
j. The guarantee measurement must exclude the savings impact from DUR programs, formulary programs, utilization management programs, and/or other therapeutic interventions.
k. Measurement will be performed annually via independent audit utilizing date-sensitive AWP derived from a single, nationally recognized price source for all claims.
B.3PBM agrees to provide upon request any proprietary algorithms, hierarchy or other logic employed to define a prescription drug as generic or brand.
C.FINANCIAL - GENERALResponse (Confirmed/Not Confirmed)
C.1PBM will invoice the State weekly for claims and once monthly for administrative services.
C.2PBM agrees to bill administration fee on a fixed-fee, per Member per month basis.
C.3There are NO additional fees (beyond those outlined in the financial section) required to administer the services outlined in this Proposal. Any mandatory fees, including clinical and formulary programs fees, must be clearly outlined in the Financial Section.
C.4All fees include the cost of claims incurred/filled during the effective dates of this contract regardless of when they are actually processed and paid (run-out).
C.5PBM agrees to review and negotiate the pricing applied to newly introduced generic drugs annually.
C.6PBM agrees to adjudicate prescription claims for compound medications with the same dispensing fees and logic associated with traditional claims.
C.7All pricing will be effective and guaranteed for the term of the agreement and will not include adjustments for claims volume shifts amongst the various provider channels (e.g., mail utilization rates decline or 90-day retail utilization increases).
C.8Confirm all pricing will be effective and guaranteed for the term of the agreement and will not be modified or amended if the State’s membership decreases by 20% or less.
C.9All applicable administrative fees will be on a per member per month basis.
C.10Each distinct pricing guarantee (including rebates) will be measured and reconciled on a component (e.g. retail brand, retail generic, retail 90 brand, retail 90 generic, mail order brand, mail order generic, specialty brand drugs at participating retail pharmacies, specialty brand drugs at the PBM’s Specialty Pharmacy, specialty generic drugs at retail, specialty generic drugs at PBM’s Specialty Pharmacy) basis only and guaranteed on a dollar-for-dollar basis with 100% of any shortfalls recouped by the State. Surpluses in one component will not be utilized to offset deficits in another component.
C.11PBM will provide a financial reconciliation report within 60 days after the end of each measurement period, and the report will include the contractual and actual discounts and dispensing fees for each component (e.g., retail brands, retail generics, mail brands, mail generics, specialty drugs via Participating Retail Pharmacies, specialty drugs via the PBM’s Specialty Pharmacy).
C.12PBM agrees that any shortfall between the actual result and the minimum guarantee will be paid, dollar-for-dollar, to the State within 90 days of the end of the measurement period.
C.13PBM ’s financial reconciliation that occurs after the end of the measurement period will use the lower of the AWP pricing at the point of adjudication or the retroactive AWP pricing, if the pricing source the PBM uses issues retroactive AWP pricing for that annual reconciliation time period.
C.14PBM agrees to the use of a single, consistent Maximum Allowable Cost (MAC) list for each drug (NDC-level). PBM agrees to share the MAC list with the State for pricing verification on a quarterly basis, and whenever new drugs are added or upon request.
C.15All pricing submitted will NOT be contingent on participation in any proposed clinical management programs, group medical or behavioral health programs proposed by you or any other vendor other than programs that are requested by the State. Further, the pricing guaranteed in the Financial Section of this RFP reflects a) the PBM’s broadest national network and b) the PBM’s proposed formulary, without mandated utilization management unless otherwise authorized or requested by the State.
C.16All pricing will NOT be contingent on specific utilization patterns. For instance, pricing terms contingent on limited utilization in a specific geographic location (e.g., Nebraska) is unacceptable.
C.17PBM will NOT implement or administer or allow any program that results in the conversion from lower discounted ingredient cost drug products to higher ingredient cost drug products without the prior written consent of the State or its designee.
C.18PBM agrees to annual Market Checks conducted by an independent third party (of the State’s choosing) to ensure the State is receiving market competitive pricing terms within the industry based on its volume and membership and will improve pricing in the event that the State’s contract terms are less than market competitive.
C.19PBM agrees to implement new pricing to commence at the beginning of the following plan year. Acceptance of the new pricing will NOT result in extension of the contract, unless requested by the State.
C.20Mail order pricing and rebates will apply to all claims that adjudicate at mail regardless of days’ supply.
C.21PBM agrees that mail order and specialty drug dispensing fees will remain constant throughout the contract term and will not be increased for any increases in postage charges.
C.22PBM will guarantee Retail/Mail Order unit cost equalization, meaning that Mail Order unit costs prior to member cost sharing, dispensing fees, and sales taxes charged to the State will be no greater than the unit cost for the same NDC-11 at Retail.
C.23PBM agrees to produce a date-sensitive comparison report showing unit costs charged to the State at a GCN-level, and reimburse the State on a dollar-for-dollar basis for all instances where mail order unit costs exceed retail unit’s costs. Report and reconciliation will be provided on an annual basis.
C.24The State will be notified of any switch in the AWP source at least 180 days prior to the change. In the event that the AWP source change is not determined by a third party to be price neutral for the State, the State will have the right to terminate the contract with no penalty.
C.25PBM will be responsible for collecting any outstanding member cost shares for prescriptions dispensed through the mail order facility. The PBM will not invoice the State for any uncollected member cost shares.
C.26The State will have the ability to adjust “refill-too-soon” limits at both retail and mail without any modifications to the guaranteed pricing.
C.27PBM agrees to provide weekly and/or monthly data transmissions to any other relevant State vendors at no charge, and two full, annual electronic claims files, in NCPDP format, at NO charge. PBM will also interact/exchange data with all vendors as required at no additional charge.
D.FINANCIAL - REBATESResponse (Confirmed/Not Confirmed)
D.1Guaranteed rebates per brand will be based on all Brand prescriptions dispensed, not only on formulary prescriptions dispensed.
D.2Rebates are guarantees on a minimum (i.e., not fixed) basis, and the PBM will pass through 100% of the rebates through to the State.
D.3Over-performance of minimum rebate guarantees will not be used to offset performance guarantee shortfalls in any other pricing guarantees.
D.4Rebates will not be withheld for execution of any contract amendments. The State is entering into a three-year agreement and needs no annual renewals/amendments signatures for payment of rebates.
D.5PBM will reconcile rebate guarantees to verify that the State is receiving the guaranteed rebates and provide rebate payments and reports listing detailed rebate utilization and calculations to the State quarterly, within sixty (60) calendar days of the quarter’s close, without a request being made by the State.
D.6PBM will provide the annual rebate report within 180 days of the end of each contract year. Any shortfall between the actual result and the minimum rebate guarantees will be paid, dollar-for-dollar, to the State within 180 calendar days of the end of the contract year.
D.7All rebate revenue earned by the State will be paid to the State regardless of its termination status as a client. Lag rebates will continue to be paid to the State after termination until 100% of earned rebates are paid.
D.8PBM agrees to produce an auditable quarterly report demonstrating pass-through rebates. PBM will attach a sample of the report they intend to use as part of their response.
E.FORMULARY MANAGEMENTResponse (Confirmed/Not Confirmed)
E.1PBM agrees to provide written notification to the State or its designee at least 90 days in advance when a Formulary drug is targeted to be moved to or from the Formulary drug list. PBM must provide a detailed disruption and financial impact analysis at the same time. No greater than five percent (5%) of Members will be disrupted by any formulary deletions or all deletions in total, on an annual basis.
E.2PBM agrees to send timely notification letters to affected Members and their prescribing physicians of drug formulary changes or other changes where there is a negative impact to Member at no additional fee.
E.3PBM agrees to remove drugs from coverage or the Formulary at most two times per year (7/1 and 1/1) and no greater than five percent (5%) of participants will be disrupted by any formulary deletions or all deletions in total, on an annual basis (except where a Generic drug is replacing a Brand drug).
F.PHARMACY NETWORK MANAGEMENTResponse (Confirmed/Not Confirmed)
F.1PBM will not withhold any financial recoveries from audits performed on the contracted pharmacy network including mail order and specialty pharmacies. Any recoveries will be disclosed and credited to the State.
F.2PBM agrees that it will not remove any participating network pharmacies that impact greater than 2% of the State’s prescriptions without communicating to the State at least sixty (60) days in advance of the scheduled change. If the change is not agreeable to the State, the State will have the right to terminate the agreement without penalty.
F.3PBM agrees to provide network geo-access reporting to the State upon request and to maintain targeted access levels throughout the contract term and such access shall include independent pharmacies throughout the State and nationally.
F.4PBM agrees to not introduce any new drug or therapeutic category limitations to any participating network pharmacies during the term of the contract.
G.AUDITING & AUDIT RIGHTSResponse (Confirmed/Not Confirmed)
G.1PBM agrees that all financial pricing components (discounts, dispensing fees, rebates) are subject to independent, electronic audit utilizing date sensitive AWP information on an NDC level from a nationally recognized pricing source (e.g., MediSpan).
G.2The State or its designee will have the right to audit annually, with an auditor of its choice, (for both claims and rebates), with full cooperation of the selected PBM, the claims, services and pricing and/or rebates, including the manufacturer or aggregator rebate contracts held by the PBM, to verify compliance with all program requirements and contractual guarantees with no additional charge from the PBM.
G.3The State or its designee will have the right to audit up to 36 months of claims data at no additional charge from the PBM.
G.4The State or its designee will have the right to audit, with an auditor of its choice, at any time provided the State gives 90-days advance notice.
G.5PBM will provide complete claim files and documentation (i.e., full claim files, financial reconciliation reports, inclusion files, and plan documentation) to the auditor within 30 days of receipt of the audit data request as long as a non-disclosure agreement is in place between the auditor and the PBM.
G.6PBM agrees to a 30-day turnaround time to provide the full responses to all of the sample claims and claims audit findings.
G.7PBM agrees to financial guarantees for turnaround times for each stage of the audit process.
G.8PBM will correct any errors that the State, or its representative, brings to the PBM’s attention whether identified by an audit or otherwise.
G.9The State or its designee will have the right to audit up to 12 pharmaceutical manufacturer contracts during an on-site rebate audit.
G.10The State’s right to audit shall survive the termination of the agreement between the parties for a period of 3 years.
G.11The State will not be held responsible for time or miscellaneous costs incurred by the PBM in association with any audit process including, all costs associated with provision of data, audit finding response reports, or systems access, provided to the State or its designee by the PBM during the life of the contract. Note: This includes any data required to transfer the business to another vendor and money collected from lawsuits and internal audits.
H.HIPAA COMPLIANCEResponse (Confirmed/Not Confirmed)
H.1PBM certifies that all personnel/staff in PBM's organization have completed their initial HIPAA training and will continue to complete HIPAA training on an annual basis.
H.2PBM will provide a copy of their most recently completed HIPAA assessment with their RFP submission.
H.3In the event of a privacy violation or data breach, PBM will provide any required remedies to resolve the violation/breach.
H.4PBM agrees to hold the State harmless for any HIPAA Violations made by the PBM and its Network Pharmacists.
I.PLAN DESIGNResponse (Confirmed/Not Confirmed)
I.1PBM agrees to duplicate the plan features and level of coverage presently offered to the State’s covered member population.
I.2PBM will ensure its proposal is issued in accordance with the specifications and information, including the full Summary Plan Descriptions (SPD) of each plan offered by the State, referenced in this RFP. PBM is required to review each plan SPD provided online at the State of Nebraska website for plan design and coverage provisions.
I.3All deviations of your ability to administer the current plan designs and coverage provisions must be CLEARLY identified. The State reserves the right to modify and/or change plan designs on an annual basis at no additional cost to the State. All deviations from the plan design requirements will be scored accordingly.
J.IMPLEMENTATION, OPEN ENROLLMENT, AND COMMUNICATIONResponse (Confirmed/Not Confirmed)
J.1PBM shall provide an implementation plan assuming a December 1, 2025 contract award. At a minimum, the Implementation Project Plan must provide specific details on the following:

a. Identification and timing of significant responsibilities and tasks

b. Names, titles, and experience of key implementation staff and time dedicated to the State during implementation

c. Identification and timing of the State's responsibilities

d. Transition requirements with the incumbent vendors

e. Staff assigned to attend and present (if required) at Open Enrollment

f. Data and timing requirements from current vendors to ensure transition of care and transfer of any open-refill, prior authorization, or other necessary files

J.2Confirm implementation will be completed prior to the State’s Annual Open Enrollment period in May 2026. The implementation plan(s) shall also define responsibilities assigned to the contractor and responsibilities assigned to the State. Failure to provide this information may be grounds to reject a proposal.
J.3After J.2, please add: Confirm that, if awarded the business, you will be prepared to start implementation work as of the contract award date due to the lead time needed for open enrollment.
J.4PBM must provide a dedicated implementation manager whose sole account is the State, who in coordination with the dedicated account manager and account management team, will effectively manage the implementation of this program. The dedicated implementation manager must continue to support the State a minimum of 60 days after the Go Live date of July 1, 2026, should the State desire. Such support includes, but is not limited to: weekly calls with the State and the designated Account Management team; maintenance of issue tracking logs; and issue resolution. This support must be provided as part of the base administrative fees with no additional cost to the State.
J.5The State requires that the PBM will be available and participate in the State’s Open Enrollment communications campaign.
J.6PBM shall provide detailed information on its procedures and time frame to prepare for annual Open Enrollment. The State will offer an annual Open Enrollment period during which time covered members may switch their plan of coverage. The successful contractor shall provide staff to assist State HR Personnel and Administrative Services – State Employee Benefits with annual Open Enrollment meetings in various locations throughout the State. The successful contractor shall have certificate books ready for distribution prior to the State’s annual Open Enrollment; State will provide plan designs electronically to Contractor 30 days prior to annual Open Enrollment. Describe your company's timelines and deadlines for Open Enrollment (system updates due to plan changes or file formats, new divisions, manual work arounds, dates for last pre-OE updates, OE file updates, etc.).
J.7PBM shall incur all costs for printing and distribution of all communications, including but not limited to:
a. Identification Cards (ID) printed
b. Booklets electronic copy provided
c. Certificates electronic copy provided
d. Summary Plan Descriptions (SPDs) electronic copy provided
J.8PBM shall incur all costs for additional open enrollment materials, including but not limited to:
a. Additional custom printing
b. Web hosting
J.9When customized printing is required, the PBM shall present a proof to the State for approval in a timely manner.
J.10PBM agrees that if they become the successful contractor that no external communications material that mentions the State's benefit plans may be circulated without written approval from the State. The State reserves the right to review, edit, or customize any communication from the PBM to its membership.
J.11PBM shall provide detailed information on how it will communicate to the members. PBM must provide sample communication materials such as certificate of coverage booklets, up-to-date-provider network directories, request letters for clinical programs, and sample EOBs.
J.12PBM shall provide members access to written or electronic EOB statements at no cost to the State or member.
J.13PBM shall produce ID cards and/or temporary proof of benefit letters in “real time”. Identification cards will be subject to final approval by the State.
J.14PBM agrees that 100% of ID cards will be distributed within 10 business days of being notified of the new or changed enrollment by the State.
J.15PBM agrees that replacement ID cards must be mailed within ten (10) business days of notification.
J.16Confirm that ID cards will be subject to final approval by the State.
J.17PBM agrees to in-person meetings with the State as required to discuss plan performance, present utilization and financial results, etc. at PBM’s expense. At a minimum, the State expects that the Account Executive and Clinical Pharmacist attend these meetings.
J.18Confirm you will provide a dedicated 24-hour toll-free customer service phone line available during Open Enrollment as well as throughout the year.
K.VENDOR ACCOUNTABILITY AND PERFORMANCE GUARANTEESResponse (Confirmed/Not Confirmed)
K.1Minimum performance standards are included in Attachment D – Performance Guarantees. PBM must provide these standards measured on State specific data. Confirm agreement.
K.2The State requires that 30% of the Administrator’s annual PBM Fees be placed at risk annually as a financial penalty for failure to meet the administrative performance guarantees in accordance with Attachment D, as established by the State of Nebraska. All penalties will be assessed based on these pre-established guarantees against actual State-specific performance results annually, not the bidder’s book of business. Confirm agreement.
K.3The State requires that 30% of the Administrator’s PBM Fees be placed at risk as a financial penalty for network discount guarantees provided by the PBM. All penalties will be assessed based on the State-specific annual performance results only. Confirm agreement.

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Questionnaire

ATTACHMENT C - CONFIRMATIONS & QUESTIONNAIREBidder:NAME
SOLICITATION NUMBER - 122436 O5
Questionnaire SectionSectionResponse
AEXPERIENCE AND REFERENCESExperienceRESPONSE
A.1Provide three references of clients. At least one reference should include a Public Sector group with at least 15,000 lives.Experience
Reference #1:Experience
a. Company NameExperience
b. Contact PersonExperience
c. TitleExperience
d. Telephone #Experience
e. E-mail AddressExperience
f. Total MembershipExperience
g. Tenure (Years)Experience
Reference #2:Experience
a. Company NameExperience
b. Contact PersonExperience
c. TitleExperience
d. Telephone #Experience
e. E-mail AddressExperience
f. Total MembershipExperience
g. Tenure (Years)Experience
Reference #3:Experience
a. Company NameExperience
b. Contact PersonExperience
c. TitleExperience
d. Telephone #Experience
e. E-mail AddressExperience
f. Total MembershipExperience
g. Tenure (Years)Experience
A.2For your entire book of business, provide the total year-end national group members. Please also provide statistics for your Public Sector clients.Experience
Total Covered Lives (excluding non-insured discount programs)Experience
2024Experience
2023Experience
Public Sector Covered Lives (excluding non-insured discount programs)Experience
2024Experience
2023Experience
Number of Public Sector ClientsExperience
2024Experience
2023Experience
Number of Public Sector Clients with 15,000+ livesExperience
2024Experience
2023Experience
A.3Explain your revenue modelExperience
A.4Do you consider your solution a transparent PBM model?Experience
a. If yes, how long have you offered a transparent PBM model?Experience
b. Do you have accounts that are not a transparent PBM model?Experience
c. If yes, what percentage of your book of business in on a non-transparent PBM model?Experience
A.5What has your average trend (claim inflation rate) been for the last 4 years, by year, for middle and enterprise market segments.Experience
A.6Does your firm participate in the business model of "claw backs" for any commercial / public plans? Please elaborate.Experience
BACCOUNT MANAGEMENTAcct MgmtRESPONSE
B.1Confirm that the proposed account management team has at least three (3) years working with Public Sector group pharmacy drug benefit plans having at least 15,000 employees.Acct Mgmt
B.2Confirm you will provide an Account Executive and a backup account staff member that will handle ALL service matters related to the operation of the program.Acct Mgmt
B.3Confirm you will respond to all State inquiries within one (1) business day.Acct Mgmt
B.4The State may require that the PBM’s Account team to attend The State's Board meetings at the PBM’s expense. Confirm understanding.Acct Mgmt
B.5How do you assess the Account Team’s performance and quality of service? Provide a sample of an annual score card or template used.Acct Mgmt
CMEMBER SERVICESMember SvcsRESPONSE
C.1The State requires a dedicated toll free number and Customer Service for this contract. This line should be dedicated solely for the use of State members.Member Svcs
a. Confirm member service representatives are available 24 hours a day, 365 days a year.Member Svcs
b. Where will this unit be located?Member Svcs
C.2Describe the process members use to transfer from the interactive voice response unit (IVR) to speak to a live representative.Member Svcs
C.3Describe your clinical pharmacist support to members, hours available, and how members reach a pharmacist.Member Svcs
C.4Confirm all member services calls are recorded and are accessible for the purposes of resolving member issues.Member Svcs
C.5Describe the system by which the Member Service unit tracks and documents calls.Member Svcs
a. Describe the process to review the findings of the call tracking and documentation process with the State.Member Svcs
b. Confirm this system is able to produce State-specific member service statistics.Member Svcs
C.6Describe your appeals procedures for denied claims or authorizations and time frames that a member would follow.Member Svcs
C.7Describe the escalation process for Member Service satisfaction and complaints.Member Svcs
C.8Describe the State of Nebraska specific website you will have available by July 1, 2026, through which members can, at a minimum, access and view eligibility, plan benefits, pharmacy and formulary information, locate a pharmacy, price a prescription specific to the State’s plan design, order a mail order refill, track a mail order shipment, and order a replacement card. This website will be linked to the State's internet home page.Member Svcs
C.9Describe your drug cost look-up tool on your member website that provides both the plan copay and full drug cost?Member Svcs
C.10Describe your mobile app features, availability, and capabilities.Member Svcs
DFORMULARY AND REBATE MANAGEMENTFormularyRESPONSE
D.1Provide a copy of your current proposed formulary (both a detailed file in Excel and an abbreviated PDF version). Provide a listing of any excluded drugs along with the preferred clinical alternatives.Formulary
D.2If requested by the State, the PBM agrees to grandfather the current formulary (preferred) list and respective copayments for up to 90 days following the contract effective date with no impact on the minimum rebate guarantees. Confirm agreement.Formulary
D.3Complete and submit a formulary disruption analysis based on your proposed formulary and the provided claims data with drug exclusions that allows for prior authorization for medical necessity. Results to be included are the number of members that will require a change as well as the number of prescriptions associated with the formulary change. An Excel file that lists the specific drugs that will be negatively impacted (excluded or higher-cost tier) along with the total number of scripts and members impacted for each of these drugs should also be provided. Please provide a summary of your formulary disruption analysis using the table below:Formulary
a. No Change:Formulary
# Members impactedFormulary
% of Total MembersFormulary
Number of Scripts ImpactedFormulary
% of Total Scripts (including all brands and generics)Formulary
b. Positive (higher-cost tier to lower tier):Formulary
# Members impactedFormulary
% of Total MembersFormulary
Number of Scripts ImpactedFormulary
% of Total Scripts (including all brands and generics)Formulary
c. Negative (lower tier to higher-cost tier):Formulary
# Members impactedFormulary
% of Total MembersFormulary
Number of Scripts ImpactedFormulary
% of Total Scripts (including all brands and generics)Formulary
d. Moving from covered to not covered/Excluded:Formulary
# Members impactedFormulary
% of Total MembersFormulary
Number of Scripts ImpactedFormulary
% of Total Scripts (including all brands and generics)Formulary
D.4Are any generic drugs considered “non-preferred” on your proposed formulary (i.e., subject to the “non-preferred” copay)? If yes, please describe in detail and provide examples.Formulary
D.5Do your manufacturer agreements contain provisions that limit the amount the manufacturer can raise the AWP price of prescription drugs each year? If yes, please describe:Formulary
D.6What reporting will you provide to the State to demonstrate such manufacturer price limit agreements provide meaningful benefits to the State?Formulary
D.7Describe the process you will use to substitute biosimilar drugs for original brand specialty drugs and include a description of reporting you will provide to demonstrate plan cost savings of the biosimilar relative to the net of rebate brand specialty drug, and conversely the net of rebate brand cost relative to the biosimilar if the brand specialty drug remains on the formulary after biosimilar availability.Formulary
D.8Do you have a formulary appeal process in place to address member concerns regarding formulary alternatives or provider indications of medical necessity? If yes, explain the process:Formulary
D.9When do formulary changes typically occur?Formulary
D.10Do you agree to limit formulary deletions up to twice per year on 01/01 and 07/01?Formulary
D.11Explain how the State and affected members will be notified about formulary changesFormulary
ECLINICAL MANAGEMENT PROGRAMS AND CAPABILITIESCMRESPONSE
E.1Confirm that you are proposing to administer the State’s clinical and other programs as outlined below. Please specify if any additional fees apply in your response below and in your response to the Financial Section of this document.CM
a. Prior AuthorizationCM
b. Step TherapyCM
c. Drug Quantity LimitsCM
d. Medication Therapy ManagementCM
e. Specialty Pharmacy ProgramCM
f. Diabetic Supplies ProgramCM
g. Vaccine AdministrationCM
E.2How will the State be kept informed of changes to clinical management rules?CM
E.3Provide a sample client management report that details clinical rule activity and savings.CM
E.4Provide a sample of your client clinical management performance report.CM
E.5Describe your PA, step therapy and quantity level limit program capabilities. Please attach a list of drug categories for which such programs can be applied.CM
E.6Provide your book-business prior authorization rate of denials for the following therapeutic categories: GLP-1, SGL-2, Specialty-Inflammatory; Specialty-Dermatology; Migraine.CM
E.7Does your firm use AI (artificial intelligence) for prior authorization approvals? If so, please provide a detailed explanation.CM
E.8Briefly describe your drug utilization review (DUR) process and indicate which point-of-sale edits can be overwritten and which are “hard” rejects. Include a list of your point-of-sale edits.CM
E.9Provide your detailed utilization management program list, including specific drugs names in each program.CM
E.10Provide a sample DUR report you produce and make available to clients.CM
E.11What was your overall average DUR savings as a percentage of plan cost in 2024? Please break-out savings by category (e.g. refill-too-soon, age restriction, etc.)CM
E.12Briefly summarize the DUR edits that detect fraud and/or abuse.CM
E.13Describe the “look-back” period (% of prescription days that must elapse) utilized for the refill-too-soon edit and indicate whether it includes only the previous claim or cumulative historical claims. Provide separately for retail and mail order.CM
E.14Can the State customize the above look back period?CM
E.15In addition to point-of-sale edits, describe any other tools or programs that are available to detect, prevent, and resolve fraud and/or abuse? Indicate whether such programs are optional and whether they entail a separate fee.CM
E.16Do you require a DEA or other identifier to be indicated to fill a controlled substance drug? If yes, how is the requirement enforced?CM
E.17Provide your standard prior authorization criteria for GLP-1 diabetes drugs.CM
E.18Describe your services to encourage drug adherence and list therapeutic categories targeted.CM
E.19Describe your policies for lost medication, vacation supplies, and overseas supplies for prescription early refills.CM
E.20Do you monitor individual physician prescribing patterns? If yes, what action is taken with physicians who have a high degree of non-compliance to improve their compliance?CM
E.21Briefly describe methods you currently have in place to influence prescribing behavior, if any. Can the State opt-in/out of these programs?CM
E.22Provide a copy of any physician score card or other reporting that is provided to clients.CM
E.23Describe your firm’s relationship with pharmaceutical and biotechnology companies.CM
E.24Provide aggregate net PMPM trend for commercial clients (> 1000 lives) by year for the last five (5) years.CM
FNETWORK ACCESS AND MANAGEMENTNetworkRESPONSE
F.1Confirm that your proposal is based on your broadest network.Network
F.2What is the current number of retail pharmacies in your network?Network
F.3List any pharmacy chains excluded from your proposed retail pharmacy network.Network
F.4Confirm you will notify plan participants, in writing, with at least 45 days advance notice (or as much time as is feasible if the terminating Pharmacy gives the Contractor less than 45 days’ notice), in the event that the contract for a participant's network pharmacy (or pharmacy chain) terminates for any reason. For the purposes of this requirement, plan participant shall mean a member who has had a prescription filled within the last 90 calendar days or a member has an active refill on file with the affected pharmacy.Network
F.5Perform and provide a GeoAccess analysis based on your contracted pharmacy network using the Census File provided. The access standards in the table below will be utilized in the analysis.Network
a. Urban / Suburban EnrollsNetwork
Pharmacy - 2 in 5 milesNetwork
b. Rural EnrolleesNetwork
Pharmacy - 1 in 15 milesNetwork
F.6Confirm you will be responsive to requests by the State to recruit additional pharmacies for the network, on a general, regional, or specific basis.Network
F.7What is the process to add a pharmacy to your network?Network
F.8Describe how you would work with the Plan Sponsor to maximize State of Nebraska employee prescriptions filled at pharmacies owned and operated by businesses in the State of Nebraska.Network
F.9Confirm you will have a network of retail pharmacies that have agreed to discount their charges for 90-day supplies of maintenance medications. PBM must provide this network through the entire term of the contract, including term extensions.Network
F.10Confirm you agree to apply MAC pricing to Retail Pharmacy 90-Day Network. The MAC price must be the same MAC as the Retail Network or better on an individual drug basis.Network
F.11Describe in detail any program available to identify and leverage low priced generic drugs available through on-line pharmacies, and how the State and members can take advantage of such pricing.Network
F.12Provide the number of participating retail pharmacies that were terminated from the network in the past 24 months: +when the termination is initiated by the PBM. ++when the termination is initiated by a pharmacy.Network
Termination Rates by Your Organization+:Network
# of PharmaciesNetwork
% of PharmaciesNetwork
Reason for TerminationsNetwork
Termination Rates by Pharmacy++:Network
# of PharmaciesNetwork
% of PharmaciesNetwork
Reason for TerminationsNetwork
F.13Confirm you will notify the State prior to anticipated major changes to the network. The State reserves the right to accept or decline proposed changes to the network and set the effective date of such changes.Network
F.14Using the Claims Repricing Data File that contains pharmacy utilization representative of the Rx utilization experience for the State’s membership, for each pharmacy listed, please indicate if the pharmacy is in the network (i.e., a participating provider) for the plan you are proposingNetwork
F.15Confirm you agree to pass through 100% of State-related audit recoveries identified through PBM's internal daily and ongoing retail network pharmacy audit compliance procedures.Network
F.16PBM must implement measures to recover overpayments made to pharmacies or members and employ a mechanism to ensure the State receives credit for these overpayments. Details of threshold recovery levels will be finalized at the time of contract award. Confirm agreement.Network
F.17List the specific network management processes currently in place to avoid fraud and abuse.Network
GMAIL ORDERMail OrderRESPONSE
G.1Please describe locations of all of your Mail Order facilities nationwide.Mail Order
G.2Confirm prescriptions purchased via mail order will never be more expensive than those obtained via retail pharmacies.Mail Order
G.3Confirm you will not repackage prescriptions or otherwise change the NDC for any prescription or OTC products dispensed at mail order.Mail Order
G.4Confirm you will communicate via a telephone call or email any delays beyond two days in the delivery of prescriptions to the member.Mail Order
G.5Confirm you will send prescription orders to members that do not provide appropriate payments with their prescription order, up to three (3) times the Plans highest copayment for each enrollee. After the ceiling is reached, the Contractor may implement standard accounts receivable policies and procedures.Mail Order
G.6Confirm you will arrange and pay for a short-term retail supply of a delayed or incorrectly processed mail order prescription caused by your organization. In addition, PBM agrees not to charge the State’s members for expedited delivery of the mail order prescription if the prescription delay is caused by PBM’s organization.Mail Order

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