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This Sources Sought opportunity was posted on April 14, 2017. The submission period has ended. Browse the details below for market research, or find similar active opportunities.

65--Request for Information - Blood Bank Reagents

Awarded
VA26317Q0515Federal

Contract Overview

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

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NAICS: 325413
New
DIBBS
CULTURE MEDIUM, THAYER-
Solicitation # SPE2DS-27-T-1066
Solicitation SPE2DS-27-T-1066 is a request for quotations issued by the DLA Troop Support Medical Supply Chain for the procurement of one package of Thayer-Martin Modified (MTM II) Agar culture medium, identified by NSN 6550-01-711-1542. This dark brown, ready-to-use plated medium is specifically designed for the isolation of pathogenic Neisseria from specimens containing mixed flora of bacteria and fungi. The product is delivered in packages of 100 plates and requires strict refrigeration storage between 2 to 8 degrees Celsius (36 to 46 degrees Fahrenheit) and must not be frozen. The contract mandates a non-extendable shelf life of three months, with a requirement that no more than 14 days elapse between the date of manufacture and the date of delivery to the government. Delivery is set for JBER, Alaska, with a required delivery date of October 27, 2026, under FOB Destination terms. Packaging must be commercial and sealed to prevent damage, with marking adhering to Medical Marking Standard No. 1 and shelf-life labels following MMS1C. Administrative requirements include electronic invoicing via the Wide Area WorkFlow system and compliance with various FAR and DFARS clauses, including the Buy American Act, Berry Amendment, and safeguarding of covered defense information. Evaluation will consider technical data for any alternate products offered and may include HUBZone price evaluation preferences. Inspection and acceptance will occur at the destination.
MEDICAL SUPPLY CHAIN MD SURG FSF

POSTED

1 day ago

DEADLINE

in 5 days
NAICS: 325413
New
Federal
6550--Optilite analyzer reagents
Solicitation # 36C26227Q0052
The Department of Veterans Affairs, Southern Arizona Healthcare System, is soliciting a Firm-Fixed Price Blanket Purchase Agreement under solicitation 36C26227Q0052 for the procurement of FDA-approved reference testing reagents and consumables validated for use on the Optilite analyzer. The scope includes specific items such as Freelite Kappa, Freelite Lambda, and Ceruloplasmin reagents, as well as TENCELL cuvettes and sample cups. To ensure system performance and safety, all materials must be manufactured by Binding Site Laboratories, and substitutions are prohibited. The contract is issued as a full and open competition under NAICS code 325413, with a total estimated period of performance of sixty months, consisting of a base period from November 9, 2026, to November 8, 2027, followed by four one-year option periods. The award will be granted to the responsible offeror whose proposal is most advantageous to the government, based on a technical acceptability review of the Statement of Work and the lowest price. Deliveries are required to be made to various VA Medical Centers across Arizona, California, and New Mexico, with standard orders delivered within four working days of placement. All shipments must be destination-based, with the vendor assuming all shipping costs and adhering to strict packaging standards to prevent damage. Invoicing is handled electronically through the Department of Veterans Affairs Financial Services Center in accordance with the Prompt Payment Act. Quotes must be submitted via email to Contract Specialist Carlos Magana by November 4, 2026.
262-NETWORK Contract Office 22 (36C262)

POSTED

3 days ago

DEADLINE

in 6 days
NAICS: 325413
New
Federal
BPA - Consumable Supplies for Terumo Trima Accel Blood Collection systems
Solicitation # HT942627QE003
The Defense Health Agency is soliciting quotations to establish a Blanket Purchase Agreement (BPA) for the recurring resupply of consumable products for three Terumo Trima Accel Blood Collection Systems used by the USAISR Combat Casualty Care Research Team 1 in Texas. To maintain FDA approval and satisfy research protocols, the contractor must provide original manufacturer-supplied consumables, including Teruflex 500ml collection bags, Trima Platelet Kits, Isoplate Solution (PAS-F), TSCD Wafers, ACD-A Solution, and 150 mL couplers. This procurement is a 100 percent set-aside for Service-Disabled Veteran-Owned Small Businesses under NAICS 325413. The resulting BPA will have a 60-month ordering period with a total ceiling of 35 million dollars, though some documentation notes a lower limit of 350,000 dollars. Individual call orders are capped at 50,000 dollars, while Government Purchase Card orders are limited to 15,000 dollars. Awards will be made on a Lowest Price Technically Acceptable basis, with technical capability rated as pass or fail. All payment requests and receiving reports must be processed electronically through the Wide Area WorkFlow system. Quotations are due by November 6, 2026, and must be submitted in two separate volumes covering technical capability and pricing.
Army Medical Resources Acq Activity

POSTED

7 days ago

DEADLINE

in 8 days
NAICS: 325413
Federal
6550--VISN Cepheid GeneXpert Testing Supplies Base Plus 3 Op Yr RFQ
Solicitation # 36C24527Q0042
The Department of Veterans Affairs, specifically the VA North Atlantic Health Network (HSA 1.3), is soliciting a firm-fixed-price, Indefinite Delivery/Indefinite Quantity (IDIQ) contract for Cepheid GeneXpert testing supplies. This requirement covers the procurement of FDA-approved reagents, consumables, and service for PCR analyzers to detect various pathogens, including CoV-2, Influenza, RSV, MRSA, and Mycobacterium Tuberculosis. The contract is structured with a base period ending October 31, 2027, and three subsequent one-year option periods extending through October 31, 2030. Deliveries will be made to multiple VA Medical Centers across Maryland, West Virginia, and Washington DC. This acquisition is set aside for HUBZone small businesses. Award will be determined using the Lowest Price Technically Acceptable (LPTA) method, evaluating technical acceptability, delivery performance, past performance, and price, with additional credit given to certified SDVOSB or VOSB offerors. Key contractor requirements include being an authorized distributor, acknowledging orders within 24 hours, and guaranteeing a minimum four-month expiration date on reagents. Additionally, the vendor must provide an emergency plan to deliver replacement supplies within 24 hours if products are found to be defective. Invoices must be submitted electronically, and payments will be processed in accordance with the Prompt Payment Act.
245-NETWORK Contract Office 5 (36C245)

POSTED

8 days ago

DEADLINE

in 6 days

AI Contract Overview

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VISN 23 is conducting market research through a Request for Information to identify capable vendors for six specific brand name blood bank reagents. The agency is seeking a single business that can provide all required products, with a particular interest in identifying Service Disabled Veteran Owned or Veteran Owned Small Business distributors. The required items include Immucor CorQC and Tech-Chek, Quotient Biodiagnostics Orr, A1, and B Cells, and Ortho Clinical Diagnostic Selectogen reagents. No substitutions or equal-to products are permitted. This effort falls under NAICS code 325413 for In-Vitro Diagnostic Substance Manufacturing and Product Service Code 6550. Interested companies must provide their business details, including DUNS number and size, along with confirmation of their ability to supply the listed reagents. This notice is issued for planning purposes only and does not constitute a formal solicitation or a binding contract.

General Info

Agency

N/A

Contract Value

$0

NAICS

325413 - In-Vitro Diagnostic Substance Manufacturing

Place of Performance

USA

Set-Aside

NONE

Awardee

AVKARE LLC

Award Issued Date

Documents

0

No documents available

Documents will appear here when they are available.

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Timeline

PhaseAwarded
Posted

Sources Sought

Awarded

Contract was awarded

Submission Closed

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Organization & Contact Information

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AgencyN/A
ContactsNo contacts available
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Office AddressN/A
ContactsNo contact information available

Full Description

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REQUEST FOR INFORMATION VISN 23 is conducting market research to compile information from businesses which offer the following six reagents. The reagents must be Brand Name Only (no substitutions or Equal-To products). The market research is multi-purpose: To identify a single business that can provide all six reagents. To identify Service Disabled, Veteran Owned, Small Business or Veteran Owned, Small Business distributors. THIS IS A REQUEST FOR INFORMATION (RFI) ONLY: The market research is looking to identify potential vendors who have the capabilities to offer the following: NAICS CODE: 325413 In-Vitro Diagnostic Substance Manufacturing Product Service Code: 6550 In-Vitro Diagnostic Substances, Reagents, Test Kits and Sets _______________________________________________________________________ 1. DESCRIPTION BRAND NAME ONLY: Immucor CorQC: Reagents for blood bank. 2.4.1.1.7. - - - - - - Quality Control of Blood Bank reagents 2.4.1.9. - CorQC reagent cells: group AB, D+ must be a 2-4% suspension with preservative to retard hemolysis and loss of antigenicity during the dating period. Used to evaluate the performance of Anti-A, Anti-B, Anti-A,B, Anti-D, and Rh control. CorQC Anti-serum: blend of polyclonal/monoclonal (murine/human) antibodies diluted with bovine albumin in physiologic saline to simulate the protein concentration of human serum. Used to evaluate serum (reverse) grouping red blood cells and antibody detection red blood cells. Prior to release, each lot of CorQC must be tested with licensed FDA reagents from two or more sources to insure that the product produces results within the ranges listed in the package insert. 2. DESCRIPTION BRAND NAME ONLY: Quotient Biodiagnostics Orr Cells: Reagents for blood bank. 2.4.1.1.7. - - - - O cell reagents for negative quality control 2.4.1.9. - O cells must be a 2-3% suspension of washed red blood cells capable of identifying agglutination due to non-ABO agglutinins. The Rh phenotype of the group O cells shall be ccdee. Prior to release, each lot of Reagent Red Blood Cells for ABO serum grouping must be tested by FDA recommended methods to confirm specificity. 3. DESCRIPTION BRAND NAME ONLY: Immucor Tech-Chek: Reagents for blood bank. 2.4.1.1.6. - - - - - - - Products for competencies 2.4.1.10. Tech-Chek must contain 2 vials per set (1 vial of unknown red blood cells and 1 vial of unknown serum) Each product is to be designed as a self-evaluation test system with different levels of complexity for testing by manual tube methods in order to help laboratory personnel develop and maintain the necessary skills in performing blood banking procedures. 4. DESCRIPTION BRAND NAME ONLY: Quotient Biodiagnostics A1 Cells: Reagents for blood bank. A1 cell reagents for serum (reverse) grouping of patients 2.4.1.1.1. Reagent Red Blood Cells 2.4.1.8. A1 must be a 2-3% suspension of washed pooled red blood cells capable of detecting Group A and Group B patients. The Rh phenotype of the group A1 and B cells shall be ccdee. Prior to release, each lot of Reagent Red Blood Cells for ABO serum grouping must be tested by FDA recommended methods to confirm specificity. 5. DESCRIPTION OBRAND NAME ONLY: Quotient Biodiagnostics B Cells: Reagents for blood bank. B cell reagents for serum (reverse) grouping of patients 2.4.1.1.1. Reagent Red Blood Cells 2.4.1.8. B Cells must be a 2-3% suspension of washed pooled red blood cells capable of detecting Group A and Group B patients. The Rh phenotype of the group A1 and B cells shall be ccdee. Prior to release, each lot of Reagent Red Blood Cells for ABO serum grouping must be tested by FDA recommended methods to confirm specificity. 6. DESCRIPTION BRAND NAME ONLY: Ortho Clinical Diagnostic Selectogen reagents: Reagents for blood bank. - - - - - - - - 2.4.1.1.4. - - - - - - - Products for antibody investigation 2.4.1.7. - Selectogen reagents (I and II) must be a 0.8% suspension of group O red blood cells in a low ionic strength diluent. Each set of Selectogens must include an ANTIGRAM Antigen Profile. The presence or absence of each antigen listed on the accompanying ANTIGRAM Antigen Profile must be tested with at least two sources of antiserum (unless rarity of antiserum precludes it). Testing must be conducted and interpreted independently. Each lot must be checked for compatibility with the ID-Micro Typing System gel test cards. If your company sells the Reagents listed above please contact me at contact@example.gov and provide the following information and any additional information that you consider pertinent: Company Name POC Phone Number Email Address Duns Business Size Product Product Product Product Product Product DISCLAIMER This RFI is issued solely for information and planning purposes only and does not constitute a solicitation. All information received in response to this RFI that is marked as proprietary will be handled accordingly. In accordance with FAR 15.201(e), responses to this notice are not offers and cannot be accepted by the Government to form a binding contract. Responders are solely responsible for all expenses associated with responding to this RFI. Jan Lang Contracting Officer contact@example.gov

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