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This Solicitation opportunity from Department Of Defense was posted on May 10, 2026. The submission period has ended. Browse the details below for market research, or find similar active opportunities.

CONTROLS, RAPID HIV-

Closed
SPE2DS-26-T-059VFederal

Contract Overview

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

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NAICS: 621410
New
DIBBS
CULTURE MEDIA, SALMONEL
Solicitation # SPE2DS-26-T-423J
Solicitation SPE2DS-26-T-423J is a request for quotations issued by DLA Troop Support Medical Supply Chain for the acquisition of Culture Media, Salmonella Shigella Agar A, including Xylose Lysine Desoxycholate Agar. The requirement is for one package consisting of ten units under NSN 6550013583835. This FDA-regulated item has a strict non-extendable shelf-life of one month and requires constant refrigeration between 2 and 8 degrees Celsius (36 to 46 degrees Fahrenheit). Delivery is required within five days after receipt of order, with FOB and inspection/acceptance points set at the destination. The contractor must adhere to rigorous packaging and marking standards, specifically Medical Marking Standard No. 1, which supersedes MIL-STD-129, and preservation standards per MIL-STD-2073-1E and special instructions MPPW00001. All units must be shipped in sealed unit containers within suitable commercial exterior shipping containers via the fastest traceable means. Invoicing and payment must be processed electronically through the Wide Area WorkFlow system. The solicitation incorporates various FAR and DFARS clauses, including those related to the Buy American Act, hazardous material labeling per 29 CFR 1910.1200, and cybersecurity requirements under NIST SP 800-171. Quotes must be submitted via the DIBBS portal by September 16, 2026.
MEDICAL SUPPLY CHAIN MD SURG FSF

POSTED

1 day ago

DEADLINE

in 5 days
NAICS: 621410
SLED
Targeted Outreach for Pregnant Women Act (TOPWA)
Solicitation # 26-003
The Targeted Outreach for Pregnant Women Act (TOPWA) initiative, administered by the Florida Department of Health's Bureau of Communicable Diseases, HIV/AIDS Section, seeks applications for FY 2027 to reduce perinatal HIV transmission and address healthcare disparities. The program focuses on early identification, engagement, and linkage to care for pregnant individuals, particularly those with substance use disorders or limited prenatal access. Key deliverables include implementing outreach plans, providing HIV, HBV, and HCV testing, linking newly diagnosed patients to medical care within 30 days, and hosting annual community baby showers. The initiative aligns with High-Impact Prevention and Ending the HIV Epidemic priorities. The anticipated contract period begins January 1, 2027, and runs through December 31, 2027, with a total potential duration of three years subject to funding availability. Approximately 1,000,000 dollars in annual funding is available. Applications are evaluated on a 120-point scale, with the highest weights given to the Program Proposal (40 points), Statement of Need (20 points), Staffing and Organizational Capacity (20 points), and Budget (20 points). Eligible applicants must provide a comprehensive electronic submission by September 30, 2026, including a project narrative, budget, and organizational documentation such as 501(c)(3) status and liability insurance. Awardees must adhere to the Florida Department of Health's non-negotiable Standard Contract and maintain strict data confidentiality and quality assurance standards.
Department of Health

POSTED

9 days ago

DEADLINE

in about 2 months

AI Contract Overview

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The contract specifies the procurement of 5 units of a Rapid HIV-1/2 Antibody Test Kit Controls, each unit containing one negative control, one HIV-1 positive control, and one HIV-2 control, designed for use with in-vitro immunological assays on whole blood, serum, and plasma. The controls are liquid, require refrigeration between 2 and 8 degrees Celsius, and have a non-extendable shelf life of six months, with at least five months remaining from the date of manufacture to the date of government delivery. The item is regulated by the FDA and must be supplied with the manufacturer's part number 1001-0077 from OraSure Technologies Inc. Packaging and marking must comply with Medical Marking Standard No. 1, which supersedes MIL-STD-129 for medical items, and all exterior shipping containers must ensure safe, cost-effective delivery via common carrier to the FPO destination for the USS THEODORE ROOSEVELT CVN 71. The product is considered non-hazardous under FED-STD-313 and must be commercially packaged per ASTM D3951, unless superseded by higher-priority DLA Master List of Technical and Quality Requirements. Delivery is due within 20 days of order placement, with FOB destination terms placing transportation risk and cost on the contractor. The contract requires full compliance with DLA packaging requirements, including palletization per RP001, and prohibits parcel post for shipment. All materials must be properly labeled with unit of issue and quantity per unit pack as specified. The solicitation calls for bidder identification of the source and part number, and buyers must confirm FDA regulatory status through a referral to the product specialist. The contract is governed by multiple FAR and DFARS clauses covering cybersecurity, information safeguarding, employment practices, whistleblower rights, and hazardous material handling. Cybersecurity compliance with NIST SP 800-171 and reporting through the Supplier Performance Risk System is mandatory, with assessments required at the Medium or High level. Invoicing must be processed via WAWF, and acceptance occurs at the destination point where government personnel perform inspection. The contract type remains to be determined by the contracting officer, and no option periods or cumulative value is specified beyond the base quantity of five units priced at $5.00 each.

General Info

Supply of FDA-regulated HIV-1/2 antibody test controls, refrigerated, 25 tests per unit, delivered within 20 days.

Agency

Department Of Defense → MEDICAL SUPPLY CHAIN MD SURG FSFView Agency

NAICS

621410 - Family Planning CentersView NAICS

Place of Performance

PR: 7016699481 PRLI: 0001 CONT’D, FPO, AP, 96632, USA

Set-Aside

NONE

Documents

(1)

RFQ SPE2DS-26-T-059V Medical Supply Chain

PDFrfq

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Timeline

PhaseClosed
Posted

Solicitation

Response Deadline

Deadline has passed

Submission Closed

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Organization & Contact Information

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AgencyDepartment Of Defense → MEDICAL SUPPLY CHAIN MD SURG FSF
Contacts1 person available
OfficeUSA
Organization / Agency
Department Of Defense → MEDICAL SUPPLY CHAIN MD SURG FSF
View Agency Profile
Office AddressUSA

Full Description

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CONTROLS,RAPID HIV
CONTROLS, RAPID HIV-1/2 ANTIBODY TEST KIT,
TEST CAPABILITY IS 25 TESTS, EACH UNIT
CONSISTS OF 1 NEGATIVE CONTROL, 1 HIV-1
POSITIVE CONTROL, 1 HIV-2 CONTROL; LIQUID
CONTROLS FOR USE WITH THE RAPID,
QUALITATIVE, IN-VITRO IMMUNO-ASSAY FOR
DETECTION OF ANTIBODIES TO HIV TYPE 1 AND
TYPE 2 IN WHOLE BLOOD, SERUM AND PLASMA.
SUITABLE FOR USE WITH END ITEMS
6550-01-526-7424 AND 6550-01-426-7431.
.
REQUIRES REFRIGERATION BETWEEN 2
AND 8 DEGREES C.
.
RS008: Shelf-life requirement RS001 for a TYPE I (CODE F) item with a shelf life of 6 months (non-extendable) applies to this item. NOT LESS THAN 5 MONTHS OF THE SHELF LIFE SHALL REMAIN FROM THE DATE OF MANUFACTURE TO THE DATE OF DELIVERY TO THE GOVERNMENT. . UNIT OF ISSUE EACH, EA . RA001: THIS DOCUMENT INCORPORATES TECHNICAL AND/OR QUALITY REQUIREMENTS (IDENTIFIED BY AN 'R' OR AN 'I' NUMBER) SET FORTH IN FULL TEXT IN THE DLA MASTER LIST OF TECHNICAL AND QUALITY REQUIREMENTS FOUND ON THE WEB AT:
http://www.dla.mil/HQ/Acquisition/Offers/eProcurement.aspx http://www.dla.mil/HQ/Acquisition/Offers/eProcurement.aspx
FOR SIMPLIFIED ACQUISITIONS, THE REVISION OF THE MASTER IN EFFECT ON THE SOLICITATION ISSUE DATE OR THE AWARD DATE CONTROLS. FOR LARGE ACQUISITIONS, THE REVISION OF THE MASTER IN EFFECT ON THE RFP ISSUE DATE APPLIES UNLESS A SOLICITATION AMENDMENT INCORPORATES A FOLLOW-ON REVISION, IN WHICH CASE THE AMENDMENT DATE CONTROLS.
RP001: DLA PACKAGING REQUIREMENTS FOR PROCUREMENT
RQ011: REMOVAL OF GOVERNMENT IDENTIFICATION FROM NON-ACCEPTED SUPPLIES
.
BIDDER SHALL SPECIFY SOURCE AND
PART NUMBER BEING SUPPLIED.
.
This device or drug is regulated by the FDA. Note to Buyers: The contracting official shall send a referral in EBS to the product specialist for confirmation. Please include bidder name and bidder contact information, manufacturer name, manufacturer part number, and item description.
APPLICABLE TO ALL MEDICAL ACQUISITIONS:
PACKAGING AND PACKING SHALL BE COMMERCIAL AS SPECIFIED IN THE PROCUREMENT DOCUMENT.
EACH COMPLETE UNIT SHALL BE PROPERLY PACKAGED IN A SUITABLE SEALED UNIT CONTAINER CAPABLE OF PROTECTING THE CONTENTS FROM DAMAGE AND/OR BREAKAGE.
UNITS SHALL BE PACKED IN SUITABLE COMMERCIAL
SPE2DS-26-T-059V
SECTION B
EXTERIOR (SHIPPING) CONTAINERS (EXPORT WHEN
NECESSARY) WHICH SHALL INSURE ACCEPTANCE AND
SAFE DELIVERY BY COMMON OR OTHER CARRIER, AT
THE LOWEST RATE, TO POINT OF DELIVERY CALLED
FOR IN THE CONTRACT OR ORDER.
MATERIAL MUST BE MARKED IAW MEDICAL MARKING
STANDARD NO. 1. THIS SUPERCEDES ALL REFERENCES
TO MIL-STD-129.
COPIES OF MEDICAL MARKING STANDARD NO. 1
(MMS NO. 1) MAY BE OBTAINED BY CONTACTING DLA
TROOP SUPPORT VIA EMAIL TO fssb@dla.mil. MMS NO. 1 IS ALSO AVAILABLE ONLINE AT: https://www.dla.mil/Logistics-Operations/Packaging/
ORASURE TECHNOLOGIES INC 0PNX6 P/N 1001-0077
DLA issues this document using the DoD authorized unit of issue, please refer to the following URL to determine the corresponding ANSI X12 unit of issue.
https://view.officeapps.live.com/op/view.aspx?src=https%3A%2F%2Fwww.dla.mil%2FPortals%2F104%2FDocuments% 2FDLMS%2FeApplications%2FLogDataAdmin%2FUnitofIssueandPurchaseUnit.xlsx&wdOrigin=BROWSELINK
CLIN PR PRLI UI QUANTITY UNIT PRICE TOTAL PRICE.
0001 7016699481 0001 EA 5.000
NSN/MATERIAL:6550015292236
DELIVERY (IN DAYS):0020
DELIVER FOB: DESTINATION
QTY VARIANCE: PLUS 0% MINUS 0%
INSPECTION POINT: DESTINATION
ACCEPTANCE POINT: DESTINATION
PREP FOR DELIVERY:
PKGING DATA-QUP:001
IF MATERIAL IS CONSIDERED HAZARDOUS IAW FED-STD-313,
PACKAGE IN ACCORDANCE WITH TQ REQUIREMENT IP025.
IF THE MATERIAL IS NOT CONSIDERED HAZARDOUS, IN ACCORDANCE WITH
FED-STD-313, THE MATERIAL SHALL BE COMMERCIALLY PACKAGED IN ACCORDANCE
WITH ASTM D3951.
All DLA Master List of Technical and Quality Requirements take precedence over ASTM D3951. Mark and label all packaging and packing in accordance with MIL-STD-129. The Unit of Issue (U/I) and Quantity per Unit Pack (QUP) will be as specified in the contract/purchase order. PALLETIZATION SHALL BE IN ACCORDANCE WITH RP001: DLA PACKAGING REQUIREMENTS FOR PROCUREMENT
PARCEL POST ADDRESS:
R21247
USS THEODORE ROOSEVELT CVN 71
UNIT 100250 BOX 3351
SPE2DS-26-T-059V
SECTION B
PR: 7016699481 PRLI: 0001 CONT’D
FPO AP 96632
US
VESSEL SHIPMENT. TRANSPORTATION SEE DLAD PROC NOTE C19. FIRST DESTINATION TRANSPORTATION SEE DLAD PROC
NOTE C20 AND CONTRACT
FREIGHT SHIPPING ADDRESS:
R21247
USS THEODORE ROOSEVELT CVN 71
DLA VENDORS: USE VSM FOR
US
RDD 777 SHIPMENT. SHIP BY FASTEST TRACEABLE MEANS. DO NOT USE PARCEL POST.
M/F: (TCN) R212476116P110
RDD: 777
PROJ: EP5 TP 2
SUPP ADD: YMH01 SIG: A
FOR GOVERNMENT USE ONLY: (IPD) 05
DIC: A4A DIST: 9B ADV: 2A FC: L7
Need Ship Date:00/00/0000 Original Required Delivery Date:05/12/2026
SPE2DS-26-T-059V NSN/Part Number: 6550-01-529-2236 Quantity: 5 EA Purchase Request: 7016699481QTY: 5 Delivery: 20 days ADO

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