This Solicitation opportunity from Department Of Defense was posted on May 7, 2026. The submission period has ended. Browse the details below for market research, or find similar active opportunities.
Department of War Pharmacy Uniform Formulary Blanket Purchase Agreement/Uniform Formulary Additional Discount Program
Contract Overview
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The Department of War, through the Defense Health Agency, is soliciting quotes from pharmaceutical manufacturers for inclusion in the Uniform Formulary under a Blanket Purchase Agreement and Additional Discount Program to support the Military Health System as mandated by 10 U.S.C. §1074g and 32 CFR §199.21. The solicitation, identified as HT9402-26-Q-9302, seeks pricing and clinical data for newly approved drugs including Lifyorli (a glucocorticoid receptor antagonist for oncology), Quiofic (a water-soluble vitamin), Widaplik (an antihypertensive), and Saphnelo (an immunosuppressive), with evaluations based on relative clinical effectiveness measured by metrics like Minimum Clinically Important Difference and Quality-Adjusted Life Years, and relative cost effectiveness using benchmarks such as Federal Supply Schedule pricing, Federal Ceiling Price, and TRICARE Retail Refund calculations. Manufacturers must submit complete NDC-11 pricing at four decimal places, package sizes, and clinical advantage documentation by the deadline of May 28, 2026, through electronic means to the designated point of contact, following templates for the UF BPA and UF ADP appendices. A pre-submission teleconference is scheduled for May 13, 2026, to clarify requirements. The Defense Health Agency in San Antonio, Texas, will administer the process, with award decisions made by the Pharmacy and Therapeutics Committee and subsequent approval by the DHA Director, leading to the establishment of agreements that govern formulary tier placement—Basic Core Formulary, Extended Core Formulary, or non-formulary—with pricing tied to quarterly retail pharmacy utilization and refund reconciliations via the TRICARE Retail Refund Website. No formal contract clauses, packaging standards beyond NDC alignment, inspection protocols, or socioeconomic set-asides are specified, and the evaluation is based on a trade-off approach rather than lowest price technically acceptable. Funding flows through program-specific mechanisms like the Industrial Funding Fee and Wholesale Acquisition Cost, without formal appropriation codes disclosed. All submissions must comply with submission formats, deadlines, and clinical data requirements, but no physical delivery, FOB terms, or quality inspection criteria are identified, as performance is transactional and tied to pharmacy benefit administration across the TRICARE network including mail-order, military treatment facilities, and retail providers.
General Info
Agency
NAICS
Place of Performance
San Antonio, TX, 78230, USASet-Aside
Timeline
Submission Closed
Organization & Contact Information
Full Description
The Department of War (DoW) is required by law (10 U.S.C. § 1074g) to establish an effective, efficient, integrated pharmacy benefits program for the Military Health System (MHS) which includes the purchase pharmaceutical agents. The law and implementing regulation (32 CFR Section 199.21) describe the process by which the DoW Pharmacy and Therapeutics (P&T) Committee will consider the relative clinical effectiveness and relative cost effectiveness of pharmaceutical agents in a therapeutic class in recommending the selection of agents for the DoW Uniform Formulary (UF) and, for cost sharing purposes, the classification of a pharmaceutical agent as generic, formulary, Basic Core Formulary (BCF), Extended Core Formulary (ECF), or non-formulary (NF). Prior to the scheduled P&T Committee meeting, a Request for Quotation (RFQ) for pharmaceutical agents within Drug Classes identified for placement on the UF has been issued to obtain quotes from industry. The Defense Health Agency may award Uniform Formulary Blanket Purchase Agreements (UF BPA) and the Uniform Formulary Additional Discount Program Agreements (UF ADP) based on the UF decision. This process is described in the attached RFQ.
P&T COMMITTEE MEETING: The following May 2026 newly approved drugs will be reviewed:
a. Lifyorli - Oncological Agents - Glucocorticoid Receptor Antagonist
b. Quiofic - VITAMINS - WATER SOLUBLE
c. Widaplik - ANTIHYPERTENSIVE AGENTS – N/A
d. Saphnelo – IMMUNOSUPPRESSIVES – N/A
The RFQ, including UF BPA and UF ADP appendices are attached here in. The instructions, important deadlines, and points of contact are in document, RFQ HT9402-26-Q-9302.
Pre-quotation teleconference is on May 13, 2026. Details are stated in Part 2.4. Pre-Quotation Teleconference. Responses to the clinical questions in Part 3.4 shall be submitted via e-mail to the RFQ POC in Part 2.3.1., no later than the date stated in Part 2.3.2.
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