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This Solicitation opportunity from Department Of Defense was posted on April 28, 2026. The submission period has ended. Browse the details below for market research, or find similar active opportunities.

CONTROL, COAGULATION

Closed
SPE2DS-26-T-026RFederal

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

2 days ago

DEADLINE

in 4 days
NAICS: 621410
SLED
Targeted Outreach for Pregnant Women Act (TOPWA)
Solicitation # 26-003
The Florida Department of Health, Bureau of Communicable Diseases, HIV/AIDS Section, is soliciting applications under RFA 26-003 for the Targeted Outreach for Pregnant Women Act (TOPWA) for fiscal year 2027. This initiative aims to reduce perinatal HIV transmission and address healthcare disparities for pregnant individuals, particularly those with substance use disorders or limited prenatal care access. The program focuses on early identification, engagement, and linkage to care, aligning with High-Impact Prevention and Ending the HIV Epidemic priorities. Key deliverables include implementing outreach plans, providing HIV, HBV, and HCV testing, linking newly diagnosed patients to medical care within 30 calendar days, and hosting annual community baby showers. The anticipated contract period begins January 1, 2027, with a total duration of three years, subject to annual 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, statement of need, staffing and organizational capacity, and budget. Eligible applicants must be non-profit or 501(c)(3) organizations and provide comprehensive documentation, including a detailed budget, organizational charts, and key personnel resumes. Submissions must be electronic, following strict formatting and page limit guidelines, and are due by September 30, 2026. Awardees must adhere to the Florida Department of Health's non-negotiable Standard Contract and comply with various federal civil rights and non-discrimination regulations.
Department of Health

POSTED

9 days ago

DEADLINE

in about 2 months

AI Contract Overview

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This contract pertains to the procurement of MICROCOAGULATION QUALITY CONTROL DIRECTCHECK, a specialized plasma control solution designed for use exclusively with HEMOCHRON JR. CITRATE PT CUVETTES to verify the accuracy of citrated prothrombin time (PT) testing. Each unit package contains fifteen vials of abnormal level control plasma alongside four protective sleeves, intended solely for quality assurance purposes in coagulation testing environments. The product requires strict refrigeration between 2 to 8 degrees Celsius (36 to 46 degrees Fahrenheit) and must not be frozen at any time to maintain integrity and performance standards. The unit of issue is PG, defined as one package of fifteen vials, and the item is classified as a TYPE I (CODE G) medical supply with a non-extendable shelf life of nine months from the date of manufacture. No more than one month may have elapsed between manufacturing and delivery to the government, with all labeling required to clearly indicate the date of manufacture, expiration or retest date, contract number, and lot number in compliance with Medical Marking Standard No. 1, which supersedes MIL-STD-129 for medical items. All packaging must adhere to commercial standards, ensuring each unit is sealed and protected against damage, and shipped in exterior containers suitable for safe transport via common carrier at the lowest cost to the specified delivery point in San Antonio, Texas. The item falls under the National Stock Number 6550-01-519-5570 and is subject to federal acquisition requirements including DLA packaging guidelines, hazard communication standards mandating Safety Data Sheets (SDS) and OSHA-compliant labeling as of June 1, 2015, and the removal of government identification from rejected supplies. Suppliers are required to submit SDS and labeling documentation for prior contracting officer approval and must ensure employee training on the Globally Harmonized System standards. The solicitation, issued under SPE2DS-26-T-026R with a response deadline of May 4, 2026, is open for bids with delivery required within five days of award, and bidders must specify the source and part number being offered to meet compliance.

General Info

Procurement of MICROCOAGULATION QUALITY CONTROL DIRECTCHECK for HEMOCHRON JR. CITRATE PT CUVETTES, refrigerated, nine-month shelf life, delivered to San Antonio by May 2026.

Agency

Department Of Defense → MEDICAL SUPPLY CHAIN MD SURG FSFView Agency

Contract Value

$138.35

NAICS

621410 - Family Planning CentersView NAICS

Place of Performance

601 DAVY CROCKETT RD, SAN ANTONIO, TX, 78226, USA

Set-Aside

NONE

Awardee

GOVERNMENT SCIENTIFIC SOURCE INCView Profile

Award Issued Date

Documents

(1)

SPE2DS-26-T-026R.pdf

PDF

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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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CONTROL,COAGULATION
,,
CONTROL,COAGULATION
MICROCOAGULATION QUALITY CONTROL DIRECTCHECK;
FEATURES ABNORMAL LEVEL PLASMA CONTROL FOR CITRATED PT;
FOR USE WITH HEMOCHRON JR. CITRATE PT CUVETTES ONLY;
EACH BOX INCLUDES 15 NORMAL LEVEL VIALS AND 4 PROTECTIVE
SLEEVES; USED AS AN ABNORMAL LEVEL CONTROL SOLUTION FOR CITRATED SAMPLES
..
REQUIRES REFRIGERATION STORAGE BETWEEN 2 TO 8 DEGREES CELSIUS
(36 TO 46 DEGREES FAHRENHEIT) DO NOT FREEZE
..
UNIT OF ISSUE: PG (15 VIALS EACH PER PACKAGE)
..
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.
..
RD003, COVERED DEFENSE INFORMATION POTENTIALLY APPLIES
..
RP001: DLA PACKAGING REQUIREMENTS FOR PROCUREMENT
..
RQ011: REMOVAL OF GOVERNMENT IDENTIFICATION FROM NON-ACCEPTED SUPPLIES
..
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
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
SPE2DS-26-T-026R
SECTION B
TROOP SUPPORT VIA EMAIL TO fssb@dla.mil. MMS NO. 1 IS ALSO AVAILABLE ONLINE AT: https://www.dla.mil/Logistics-Operations/Packaging/
.. RS009: Shelf-life requirement RS001 for a TYPE I (CODE G) item with a shelf life of 9 months (non-extendable) applies to this item.
SHALL HAVE A SHELF LIFE OF 9 MONTHS. NOT MORE THAN 1 MONTH SHALL HAVE ELAPSED FROM DATE OF MANUFACTURE TO DATE OF DELIVERY TO THE GOVERNMENT. . SHELF LIFE MARKINGS SHALL BE IN ACCORDANCE WITH THE LATEST REVISION OF MMS1C.
. ALL LABELS SHALL INCLUDE:
DATE OF MANUFACTURE, EXPIRATION, OR RETEST DATE CONTRACT NUMBER/LOT NUMBER. .. RQ034: HAZARDOUS COMMUNICATION STANDARD NOTICE
Hazard Communication Standard Notice:
Effective June 1, 2015, Federal Standard No. 313-E, Material Safety Data, Transportation Data and Disposal Data for Hazardous Materials Furnished to Government Activities, establishes the requirement for preparation and submission of Safety Data Sheets (SDS) in lieu of Material Safety Data Sheets (MSDS) by suppliers who provide hazardous materials to government activities.
The Occupational Safety and Health Administration (OSHA) has modified its Hazard Communication Standard (HCS) to conform to the United Nations Globally Harmonized System of Classification and Labeling of Chemicals. As a result of this change, GSA revised Federal Standard No. 313-E requiring Safety Data Sheets for classifying chemicals and communicating the applicable information on labels.
In accordance with the revised standard after June 1, 2015:
1. Suppliers will be required to submit, to the contracting officer for review and approval prior to award, safety data sheets consistent with the requirements found at 29 C.F.R. 1910.1200 for hazardous materials delivered to the Government.
2. Suppliers will also be required to submit, to the contracting officer for review and approval prior to award, Hazardous Communication Standard (HCS) labels in accordance with 29 C.F.R. 1910.1200 requirements or current Consumer Product Safety Act (CPSA), Federal Hazardous Substance Act (FHSA) labels when subject to labeling requirements under those statutes. This product labeling is required for hazardous materials delivered to the Government.
3. Finally, suppliers must train their employees on the new safety data sheets, hazardous communication labels, and requirements of 29 C.F.R. 1910.1200.
For more information on SDS, refer to OSHAs website, available at:
https://www.osha.gov/law-regs.html
For information on 29 C.F.R. 1910.1200, refer to the below link:
https://www.osha.gov/dsg/hazcom/index.html .. BIDDER: PLEASE SPECIFY SOURCE AND PART NUMBER BEING SUPPLIED.
ADEQUATE DATA FOR THE NSN/Part Number: 6550-01-519-5570 Quantity: 1 PG Purchase Request: 7016543960QTY: 1 Delivery: 5 days ADO

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