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This Combined Synopsis/Solicitation opportunity from Department Of Health And Human Services was posted on September 16, 2026. The submission period has ended. Browse the details below for market research, or find similar active opportunities.

Animal Blood

Closed
CDRH2026134634Federal

Contract Overview

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

Active Opportunities Like This One

NAICS: 325414
New
International
Реагенти для лабораторії імуногенетичних технологій та біоінженерії – ДК 021:2015 – 33690000-3 - Лікарські засоби різні (КЛІТИННА ЛІНІЯ Nalm-6-Zellen – Код ДК 021:2015 – 33696500-0 - Лабораторні реактиви (НК 024:2023/НК 031:2024 – 30670 - Лінія клітинної
Solicitation # UA-2026-11-06-013516-a
The National Children's Specialized Hospital Okhmatdyt of the Ministry of Health of Ukraine is soliciting bids for the procurement of laboratory reagents, specifically the Nalm-6 cell line, for the Laboratory of Immunogenetic Technologies and Bioengineering. This solicitation, identified by number UA-2026-11-06-013516-a, is categorized under various medical and laboratory reagent codes. The performance of the contract and delivery of goods will take place in Kyiv, Ukraine. Interested parties must submit their responses by the deadline of November 22, 2026. A critical compliance requirement for this contract is that the goods provided cannot originate from the Russian Federation, the Republic of Belarus, or the Islamic Republic of Iran. Primary contact for this procurement is Maryna Yakymchuk.
Державне некомерційне підприємство «Національна дитяча спеціалізована лікарня «Охматдит» МОЗ України»

POSTED

2 days ago

DEADLINE

in 14 days
NAICS: 325414
New
DIBBS
MEDICAL PHARMACY EMERGENCY NON NSN ORDER
Solicitation # SPE2DP-26-R-0004
Solicitation SPE2DP-26-R-0004 is a Request for Proposal issued on November 4, 2026, by the Department of Defense Medical Supply Chain Pharmacy FSA for the procurement of egg-free Influenza Virus Vaccine, 2027-2028 Formula for adults aged 18 and older. The government intends to award a Firm Fixed Price, Indefinite Delivery, Indefinite Quantity contract to the responsible offeror determined to be most advantageous based on price and non-price factors. Proposals must be submitted electronically via the DIBBS system by December 3, 2026. Award criteria include the proposed unit and total price, agreement to all solicitation terms without exception, and, for large businesses, the submission of a Small Business Subcontracting Plan. The contract mandates strict quality and cold chain management standards, requiring vaccines to be maintained between 2 to 8 degrees Celsius during transportation for up to 72 hours with no acceptable excursions. Products must be delivered to DLA Distribution Susquehanna in New Cumberland, Pennsylvania, and must have an expiration date no later than 18 months after the date of issue from the manufacturer's cold storage. Manufacturers must be FDA current Good Manufacturing Practice acceptable. Packaging and marking must adhere to Medical Marking Standard No. 1D and MIL-STD-129 for perishables. Invoicing and payment will be processed electronically through the Wide Area Workflow system.
MEDICAL SUPPLY CHAIN PHARM FSA

POSTED

4 days ago

DEADLINE

in 25 days
NAICS: 325414
Federal
Foot and Mouth Disease (FMD) Vaccine Antigen Concentrate (VAC)
Solicitation # 12639527R0001
Solicitation 12639527R0001 is a request for proposal issued by the USDA Animal and Plant Health Inspection Service (APHIS) for an unrestricted, IDIQ contract focused on Foot and Mouth Disease (FMD) Vaccine Antigen Concentrate (VAC). The scope of work includes the purchase and storage of VAC, the conversion of Government-owned VAC into usable finished vaccines, and the direct purchase of finished vaccines. The contract features a ceiling price of 800 million dollars and a long-term performance horizon, consisting of five one-year ordering periods for VAC and direct purchases starting December 1, 2026, with conversion and delivery of finished vaccines extending through November 30, 2044. The contractor is required to produce VAC with a minimum capacity of 1.0 million doses and maintain storage on their premises under strict quality control and temperature monitoring standards. Due to the nature of the material, live FMDV is classified as a Tier 1 Select Agent, requiring specific authorization from the CDC/APHIS and adherence to rigorous shipping and security restrictions. Award will be based on the most advantageous offer, evaluating technical capability, past performance, and price, with technical and past performance factors weighted equally. Proposals must be submitted electronically in four separate volumes by November 10, 2026.
Mrpbs Minneapolis Mn

POSTED

12 days ago

DEADLINE

in 2 days

AI Contract Overview

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Solicitation 75F40126Q00362 is a Request for Quotation issued by the FDA Center for Devices and Radiological Health for the procurement of donor animal whole blood, specifically bovine, ovine, and porcine species. These products are required to support medical device research and blood compatibility testing, including projects focused on hemolysis and thrombosis. The contract is a total small business set-aside under NAICS code 325414. The performance period consists of a base year running from October 1, 2026, to September 30, 2027, with four subsequent option years extending through September 30, 2031. The contractor must provide whole blood with ACD-A or Na Heparin, ensuring that products are bled and shipped on the same day. Strict technical requirements include AALAC accreditation, ISO 13485:2016 certification, veterinary oversight, and adherence to specific quarantine and labeling protocols. Deliveries are made to the Office of Science and Engineering Laboratories in Silver Spring, Maryland, with inspection and acceptance occurring at the destination. Award is based on a best-value tradeoff, weighing technical capability and past performance approximately equal to price. Invoicing must be processed electronically through the U.S. Department of Treasury's Invoice Processing Platform.

General Info

FDA seeks small business for donor animal whole blood for medical device research.

NAICS

325414 - Biological Product (except Diagnostic) Manufacturing

Place of Performance

Silver Spring, MD, 20903, USA

Set-Aside

SBA

Documents

1
PDF, High priority: read this firstrfq
High

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Timeline

PhaseClosed
Posted

Combined Synopsis

Response Deadline

Deadline has passed

Submission Closed

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Organization & Contact Information

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AgencyDepartment Of Health And Human Services → FDA Office Of Acq Grant Svcs
Contacts1 person available
OfficeRockville, MD, 20852, USA
Office AddressRockville, MD, 20852, USA

Full Description

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This is a synopsis of a procurement for commercial products prepared in accordance with the commercial acquisition procedures of RFO Part 12.


Solicitation No. 75F40126Q00362 was issued as a Request for Quotation (RFQ) for donor animal whole blood (bovine, ovine, and porcine) for the FDA Center for Devices and Radiological Health (CDRH), Office of Science and Engineering Laboratories (OSEL), Cardiovascular Program, Division of Applied Mechanics (DAM). The blood products support blood compatibility (hemocompatibility) testing and medical device research, including hemolysis- and thrombosis-related projects, as further described in Attachment 1 – Requirements Document.


All supplies shall meet the minimum requirements in Attachment 1 – Requirements Document, including species availability, minimum draw frequency, blood quality, minimum delivery volumes, anticoagulant type, labeling, quarantine protocol, veterinary oversight, AAALAC accreditation, and ISO 13485:2016 certification.

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POSTED

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DEADLINE

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NAICS: 541611
New
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FDA/CDRH Scientific Technical Capacity for Regulatory Review
Solicitation # 75F40127Q00006
The FDA Center for Devices and Radiological Health (CDRH) has issued a Sources Sought Notice under solicitation 75F40127Q00006 to conduct market research for a Blanket Purchase Agreement. The objective is to secure advanced professional and scientific consultants to provide technical capacity for regulatory reviews across the total product lifecycle of medical devices. Required expertise spans a vast array of disciplines, including biomedical engineering, computer science, cybersecurity, data science, and various clinical specialties such as anesthesiology, toxicology, and virology. These consultants will support critical activities including research, digital health consultations, auditing, and the evaluation of the safety and effectiveness of devices approved, cleared, or authorized by the FDA. The anticipated period of performance includes a twelve-month base year starting January 30, 2027, followed by four twelve-month option years and a final six-month extension option ending July 29, 2032. Services will be performed both remotely via the FDA network and on-site at the White Oak Headquarters in Silver Spring, Maryland. The government is considering NAICS code 541611 for this effort and is seeking information from large and small businesses, including various socio-economic categories. Interested vendors must submit their responses, including a completed Vendor Feedback Form and capability statement, to the designated contract specialists by 2:00 PM EST on November 17, 2026.
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