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This Government Contract opportunity from Department Of Defense was posted on September 1, 2026. The submission period has ended. Browse the details below for market research, or find similar active opportunities.

Notice of Intent to Sole Source - EzPlaz

Closed
HT942726QE015Federal

Contract Overview

Solicitation details, issuing organization, response deadlines, documents, and interested companies for this government contract opportunity.

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NAICS: 325412
New
DIBBS
Epinephrine Injector
Solicitation # SPE2D2-26-R-0009
Solicitation SPE2D2-26-R-0009 is a federal procurement issued by the Defense Logistics Agency Troop Support Medical Supply Chain for the acquisition of Epinephrine 0.3 MG/0.3 ML Injection Auto-Injectors in 2-count boxes. The government is seeking offers from manufacturers or distributors to ensure an uninterrupted supply, with a total contract duration not to exceed five years. The procurement is conducted as a lowest price technically acceptable acquisition, where awards are based on technical acceptability regarding requirements and past performance, followed by the lowest evaluated aggregate price. The estimated quantity for the base year and subsequent option years is 473,905 boxes per period. Offerors must submit their proposals electronically via DIBBS by November 16, 2026. Required documentation includes a signed SF 1449, a price proposal, and either a Letter of Certification for manufacturers or a Letter of Commitment from the manufacturer for dealers and suppliers. Strict quality and regulatory standards apply, including mandatory FDA clearance and compliance with current Good Manufacturing Practices. Packaging must feature child-proof closures, non-glass bottles with a minimum 100cc volume, and GS1-128 or HIBC compliant bar coding at the unit-of-use level encoding the National Drug Code. All contractors must also adhere to the Drug Supply Chain Security Act and various FAR and DFARS clauses regarding trade agreements and cybersecurity.
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Febuxostat Tablets
Solicitation # SPE2D2-26-R-0012
Solicitation SPE2D2-26-R-0012 is a requirements contract issued by the Defense Logistics Agency Troop Support Medical Supply Chain for the procurement of Febuxostat tablets in 30-count bottles. The requirement covers two strengths: 40mg and 80mg tablets. The acquisition is conducted as a Lowest Price Technically Acceptable (LPTA) procurement, where the award is granted to the responsible offeror who is determined to be technically acceptable and provides the lowest evaluated aggregate price. Technical acceptability is based on compliance with the Statement of Work and a review of past performance, including the status of FDA warning letters, violations, or failed inspections. The contract mandates strict adherence to FDA current Good Manufacturing Practice (cGMP) standards and requires products to have valid New Drug Applications (NDA) or Abbreviated New Drug Applications (ANDA), specifically preferring a Therapeutic Equivalence Code of A. Packaging must meet precise specifications, including a cylindrical bottle with a minimum 100cc volume, a 5.75-inch minimum circumference, and a child-proof safety cap. Labeling must be GS1-128 or HIBCC compliant and include linear bar coding at the unit-of-use level. Offers must be submitted exclusively through the Defense Logistics Agency Internet Bid Board System (DIBBS). Following several amendments, the final closing date for the receipt of offers is October 29, 2026, at 3:00 PM EST. Proposals must be organized into a non-price volume and a price proposal volume, including a Letter of Certification on manufacturer letterhead and specific FDA disclosures. The contract structure includes a base year and four option years, with an estimated base quantity of 76,388 bottles for the 40mg tablets.
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NAICS: 325412
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6505--Lab Supplies - Radiopharm Philadelphia VA Medical Center
Solicitation # 36C24427Q0018
The Department of Veterans Affairs Network Contracting Office 4 is soliciting quotations for an indefinite-quantity contract to provide radiopharmaceuticals and calibration sources for the Nuclear Medicine Department at the Corporal Michael J. Crescenz VA Medical Center in Philadelphia, Pennsylvania. The contract covers a base period from November 1, 2026, to October 31, 2031, with four additional option years. The selected vendor must be licensed and accredited by the Nuclear Regulatory Commission and comply with all regulations from the DOT, FDA, OSHA, and NHPP. Key deliverables include various cold kits and specific radiopharmaceuticals, with strict delivery requirements: routine orders must be received by 8:00 AM the following workday, and same-day orders must be delivered within two hours during normal business hours. The government will award the contract based on a comparative evaluation of price and past performance from the last three years, utilizing simplified acquisition procedures for commercial products. Technical requirements include specific labeling for radioactive materials and unit doses, as well as the provision of bar-labeled inserts for integration with the PineStar nuclear medicine information management system. If the contractor's system differs, they must provide data migration and training at no additional cost. Invoicing is to be submitted monthly and electronically via the Austin Payment Center. The solicitation is unrestricted, though price evaluation preference is provided for HUBZone small business concerns.
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AI Contract Overview

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The Defense Health Agency intends to award a firm-fixed price Indefinite Delivery/Indefinite Quantity contract to Vascular Solutions LLC on a sole source basis. This action is driven by a critical requirement for FDA approved Freeze Dried Plasma for transfusions when other plasma products are unavailable. Vascular Solutions LLC is identified as the only source capable of meeting these requirements, as their product, EZPLAZ, is the first and only licensed FDP product currently on the market. While the agency intends to proceed with a sole source award, it is issuing this notice to determine if other competitive sources exist. Interested parties must submit a capability statement including technical, management, and cost data by September 16, 2026, to demonstrate their ability to provide an FDA approved FDP product. These submissions must be sent via email to the designated points of contact and must not exceed five pages. If no qualifying responses are received, the contract will be awarded to Vascular Solutions LLC without further notice.

General Info

DHA seeks alternative FDA approved Freeze Dried Plasma providers to avoid sole source contracting.

NAICS

325412 - Pharmaceutical Preparation Manufacturing

Place of Performance

MD, 21702, USA

Set-Aside

NONE

Documents

0

No documents available

Documents will appear here when they are available.

AI Contract Breakdown

Uniform Contract Format

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Timeline

1 update
PhaseClosed
Posted

Sources Sought

Notice updated

Notice type changed from Sources Sought to Special Notice. Response deadline changed from Sep 1, 2026 to Sep 16, 2026. The notice title changed. The notice description changed.

Response Deadline

Deadline has passed

Submission Closed

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Organization & Contact Information

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AgencyDepartment Of Defense → Defense Health Agency
Contacts2 people available
OfficeFORT DETRICK, MD, 21702, USA
Office AddressFORT DETRICK, MD, 21702, USA
Contacts
Timothy Kelly
Shannon Lertora

Full Description

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The Defense Health Agency (DHA) Contracting Activity (DHACA), on behalf of the DHA’s Portfolio Acquisition Executive Medical Products (PAE MP), intends to issue a firm-fixed price Indefinite Delivery/Indefinite Quantity contract on a sole source basis under the authority of the Revolutionary Federal Acquisition Regulation (FAR) Overhaul, FAR 6.103-1, only one responsible source and no other supplies or services will satisfy agency requirements, to Vascular Solutions LLC, 6420 Sycamore Ct N, Maple Grove, Minnesota 55369-6032.



Vascular Solutions, LLC is the only source able to meet the Government’s requirements. The Government has a has a critical requirement for supply of a Food and Drug Administration (FDA) approved Freeze Dried Plasma (FDP) product for transfusion when plasma is required and other plasma products are not available. The FDA approved Vascular Solutions, LLC FDP product, EZPLAZ™, on 29 July 2026. Vascular Solutions LLC holds the first and only FDA-approved (licensed) FPD product on the market.



This Notice of Intent is not a request for competitive proposals and no solicitation document exists for the requirement.  Sources interested in responding to this notice are required to submit a capability statement that includes management and technical data and cost information, in sufficient detail and with convincing evidence that clearly demonstrates the capability to perform the required work.  Responses must be supported with clear and convincing evidence articulating the ability to provide FDA approved FDP product. Capability statements shall not exceed 5 (8.5 x 11 inch) pages using a font size no smaller than 10-point.  All capability statements received by the due date of this notice will be considered by the Government.  A request for documentation or additional information or submissions that only ask questions will not be considered as an affirmative response.  A determination by the Government not to compete based on responses to this notice is solely within the discretion of the Government.  Information received will be considered solely for the purpose of determining whether to conduct a competitive procurement or to proceed with a sole source contract. If no written responses are received by the date listed below, an Indefinite Delivery/Indefinite Quantity contract will be awarded without further remark.



Capability statements are due by 3:00 PM local time, 16 September 2026. Capability statements shall be submitted by e-mail ONLY as a Microsoft Word or Adobe PDF attachment to the following address: timothy.j.kelly169.civ@health.mil and shannon.p.lertora.civ@health.mil.

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