This Government Contract opportunity was posted on September 27, 2019. The submission period has ended. Browse the details below for market research, or find similar active opportunities.

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Immunoassay Control Kits

Awarded

W81K0019Q0239Federal

Submission Closed09/26/2019, 12:00:00 AM UTC

Contract Overview

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

Active Opportunities Like This One

NAICS: 325413

New

DIBBS

TEST KIT, CORONAVIRUS D

Solicitation # SPE2DS-27-T-1071

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MEDICAL SUPPLY CHAIN MD SURG FSF

POSTED

DEADLINE

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

DEADLINE

Supply of ALBAcyte Blood Bank ReagentsThis subcontract involves the manufacture and supply of specialized ALBAcyte blood bank reagents for prime contractors supporting the Department of Veterans Affairs North Texas Health Care System. The scope of work includes the delivery of A1, A2, B, IgG Sensitized, Antibody ID Panels, and C3 Coated RBCs. To ensure product efficacy, the contractor must utilize shipping containers that maintain reagent integrity and adhere to a defined Quality Plan and FDA approval standards. Deliveries are to be made FOB Destination to the Transfusion Medicine Unit located in Dallas, Texas. The contract is categorized under NAICS code 325413 and is managed through the Department of Veterans Affairs Network Contract Office 17.

257-NETWORK Contract Office 17 (36C257)

POSTED

DEADLINE

6550--Blood Bank Reagents

Solicitation # 36C25727Q0065

The Department of Veterans Affairs VA North Texas Health Care System is issuing a Sources Sought Notice to identify qualified vendors capable of providing blood bank reagents for the Transfusion Medicine Unit in Dallas, Texas. These reagents, including ALBAcyte A1, A2, B, IgG Sensitized, Antibody ID Panels, and C3 Coated Red Blood Cells, are essential for manual blood typing and serum antibody detection used in cross-matching blood for transfusions. The anticipated acquisition strategy includes a base year starting May 1, 2027, with four subsequent one-year option periods extending through April 30, 2032. To be considered, vendors must be FDA approved, provide documentation of such approval, and maintain a defined quality plan with adequate supply availability. All shipments must be FOB Destination, and the contractor is responsible for providing appropriate shipping containers. Interested vendors must submit an electronic capability statement in PDF or Word format, including the place of manufacture for all listed reagents, to the designated contract specialist by November 5, 2026, at 9:00 AM CST. This notice is for market research purposes only to determine the appropriate acquisition strategy, such as a small business set-aside, and does not constitute a formal solicitation.

257-NETWORK Contract Office 17 (36C257)

POSTED

DEADLINE

6505--DRESSING, DRAWTEX 4IN X 4IN (VA-27-00014447)

Solicitation # 36C77027Q0015

The Department of Veterans Affairs, National CMOP Office, is conducting market research through a Sources Sought announcement to identify qualified sources for the procurement of Drawtex Dressing, 4in X 4in, packaged as 10ct per box. This action is for market research purposes only and is not a formal solicitation for quotes; therefore, no contract will be awarded based on this specific announcement. The place of performance is located in Ladson, South Carolina, and the primary point of contact is Contract Specialist Claudine Challinor. Interested respondents must submit their information via email by November 3, 2026. Required details include the company's SAM Unique ID Number, business size (Small, Large, SDVOSB, or VOSB), and point of contact information. Specifically, the government is seeking to determine if the respondent is the manufacturer, the manufacturer's product number, and the place of manufacturing. If the respondent is not the manufacturer, they must provide a letter of authorization from the original equipment manufacturer or provide detailed product literature and specifications for alternative products that demonstrate similarities to the Drawtex hydro conductive wound dressing.

National Cmop Office (36C770)

POSTED

DEADLINE

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

DEADLINE

Supply of i-STAT PT Plus Control Reagent Level 1This subcontract involves the procurement and delivery of i-STAT PT Plus Control Reagent Level 1 for coagulation testing to support prime contractors fulfilling Department of Defense supply contracts. The scope of work requires the delivery of two boxes, each containing ten 1.0 mL units, shipped FOB Destination to a performance location in APO 96260-5479. To ensure quality and safety, all supplied reagents must adhere to Regulation 864.7750 Class II requirements and maintain full compliance with Registration, Listing, Labeling, and Good Manufacturing Practices. This requirement is managed under NAICS code 325413 for the Medical Supply Chain MD Surg FSF agency.

MEDICAL SUPPLY CHAIN MD SURG FSF

POSTED

DEADLINE

CONTROL SET, BLOOD CHEM

Solicitation # SPE2DS-27-T-0906

Solicitation SPE2DS-27-T-0906 is a request for quotations from DLA Troop Support for two sets of DXH 500 Series Blood Chemistry Control (NSN 6550-01-688-9090). This assayed whole blood control is used to monitor multi-parameter hematology cell counters and includes abnormal low, normal, and abnormal high components. The items must be stored refrigerated and upright between 2 to 8 degrees Celsius and protected from freezing and overheating. Delivery is required within 20 days after receipt of order, with a required delivery date of October 27, 2026, under FOB Destination terms. The contract imposes strict shelf-life requirements, specifying a non-extendable shelf life of 3 months, with no more than 13 days elapsed from the date of manufacture to the date of delivery. Packaging must be commercial and compliant with RP001 and MIL-STD-2073-1E, while marking must adhere to Medical Marking Standard No. 1. Invoicing is to be processed electronically via the Wide Area Workflow system. This is not a small business set-aside, and the procurement falls under NAICS code 325413. Compliance with the Buy American and Balance of Payments Program and DFARS safeguarding of covered defense information is required.

MEDICAL SUPPLY CHAIN MD SURG FSF

POSTED

DEADLINE

CONTROL, BLOOD CHEMISTR

Solicitation # SPE2DS-27-T-0950

Solicitation SPE2DS-27-T-0950 is a Request for Quotations issued by the Department of Defense, DLA Troop Support Medical Supply Chain, for the procurement of two boxes of i-STAT PT Plus Control Reagent Level 1 (NSN 6550-01-728-5703). This reagent is used for coagulation testing and is compatible with the i-STAT PT Plus cartridge and the i-STAT 1 Government Field Kit analyzer. Each box contains ten 1.0 mL units. The required delivery date is October 23, 2026, with a delivery window of 83 days after award. Inspection and acceptance will occur at the destination per FAR 52.246-2. The contract mandates strict quality and storage requirements, including refrigeration between 2 to 8 degrees Celsius and a non-extendable shelf life of 12 months. Items must be delivered within one month of the manufacture date. Packaging must be commercial and adhere to MIL-STD-2073-1E and RP001, with marking compliant with Medical Marking Standard No. 1. Labels must include the contract/lot number and manufacture or expiration dates. The procurement is not a small business set-aside, though a HUBZone price evaluation preference may be applied. Compliance with the Buy American Act and DFARS domestic material restrictions is required, and electronic invoicing must be processed through the Wide Area WorkFlow system.

MEDICAL SUPPLY CHAIN MD SURG FSF

POSTED

DEADLINE

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

DEADLINE

Custom ArcherDX VariantPlex NGS Target-Enrichment KitsThis subcontract involves the supply of custom-designed Next-Generation Sequencing target-enrichment library preparation kits to support prime contractors on NIH NHLBI projects. The required kits must be manufactured using proprietary ArcherDX VariantPlex Anchored Multiplex PCR chemistry and pre-amplification ligation of unique molecular barcodes. To ensure operational compatibility, all delivered kits must function with Archer Analysis software and Illumina NovaSeq instruments. Managed under the National Institutes of Health Olao within the Department of Health and Human Services, the contract falls under NAICS code 325413. The procurement process began with a posting date of October 22, 2026, and established a response deadline of November 2, 2026.

National Institutes Of Health Olao

POSTED

DEADLINE

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

7 days ago

DEADLINE

in 7 days

General Info

Agency

N/A

Contract Value

$175,731.08

NAICS

325413 - In-Vitro Diagnostic Substance Manufacturing

Place of Performance

San Antonio Military Medical Center (SAMMC), Joint Base San Antonio-Fort Sam Houston., SAN ANTONIO, TX, 78234, USA

Set-Aside

NONE

Awardee

BIO RAD LABORATORIES INC

Award Issued Date

10/01/2019, 12:00:00 AM UTC

Documents

No documents available

Documents will appear here when they are available.

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Uniform Contract Format

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Timeline

2 updates

PhaseAwarded

PostedJul 18

Sources Sought

Type ChangedAug 8

Sources Sought → Presolicitation

Notice updatedAug 20

Response deadline added: Sep 3, 2019. The notice description changed.

Notice updatedSep 4

Response deadline changed from Sep 3, 2019 to Sep 9, 2019. The notice description changed.

Type ChangedSep 9

Presolicitation → Solicitation

AwardedOct 1

Contract was awarded

Submission Closed

09/26/2019, 12:00:00 AM UTC

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Organization & Contact Information

AgencyN/A

Contacts1 person available

OfficeN/A

Organization / Agency

N/A

Office AddressN/A

Contacts

Rosalba MartinezContract Specialist

contact@example.gov

+1 (555) 000-0000

Full Description

The purpose of this sources sought notice is to conduct market research to determine if responsible sources exist by ascertaining if this effort can be successfully competed and/or set-aside for Small Businesses. The proposed North American Industry Classification System (NAICS) Code is 325413 - In-vitro Diagnostics Substance manufacturing with a corresponding size standard of 1,250 employees. The Government will use this information to determine the best acquisition strategy for this procurement. The Government is interested in all large and small businesses to include 8(a), Service-Disabled Veteran- Owned, HubZone, and Women-Owned small business concerns. The Regional Health Contracting Office - Central, JBSA, Fort Sam Houston, Texas, is seeking potential sources to provide Immunoassay Control Kits for precision of Immunoassay reagents, Department of Pathology and Area Laboratory Services, San Antonio Military Medical Center, JBSA - Fort Sam Houston, TX. Immunoassay reagents measure the concentration of molecules in a solution through the use of an antibody/immunoglobin. 1) Organization name, address, e-mail address, Web site address, telephone number, and size (small versus large business, and any other socio-economic categories) and type of ownership for the organization; 2) Tailored capability statements addressing the salient characteristics listed, with appropriate documentation supporting capability. The Vendor shall be able to provide material to cover all analytes listed. The Vendor shall be able to supply a local or internet based expert quality control program which can utilize data as provided by the Roche instruments via the Data Innovations Instrument Manager middleware. The Quality Control program shall be able to provide a report comparing the affiliated hospitals and clinics. The Quality Control Program shall provide interlaboratory peer group comparisons. The Quality Control program shall be able to load the latest peer comparisons that can be compared to labs values on Levy Jennings Charts. The Vendor agrees to supply the customer with the following control material. All material must meet or exceed the following specifications. 1. Liquichek Cardiac Marker Plus Control LT Level 1(Product No. 146) or equivalent: Shall be liquid, human serum based, ready to use. Shall have 20 day open vial stability at 2-8C for most analytes. Package of 6 x 3 mL. Shall have the following analytes: CK (Total), Digitoxin, NT-proBNP CKMB, Homocysteine, Troponin I, CRP, Myoglobin, Troponin T 2. Liquichek Cardiac Marker Plus Control LT Level 3(Product No. 148) or equivalent: Shall be liquid, human serum based, ready to use. Shall have 20 day open vial stability at 2-8C for most analytes. Package of 6 x 3 mL. Shall have the following analytes: CK (Total), Digitoxin, NT-proBNP CKMB, Homocysteine, Troponin I, CRP, Myoglobin, Troponin T 3. Liquichek Diabetes Control Level 1(Product No. 171) or equivalent: Shall be liquid, human whole blood based, ready to use. Shall have 6 month shelf life and 14 day open vial stability at 2-8C. Package of 6 x 1 mL. Shall have the following analytes: Hemoglobin A1C, Hemoglobin (Total) 4. Liquichek Diabetes Control Level 3(Product No. 173) or equivalent: Shall be liquid, human whole blood based, ready to use. Shall have 6 month shelf life and 14 day open vial stability at 2-8C. Package of 6 x 1 mL. Shall have the following analytes: Hemoglobin A1C, Hemoglobin (Total) 5. Liquichek Pediatric Control Level 2(Product No. 355) or equivalent: Shall be human serum based, liquid, ready to use. Shall have at least 14 day open vial stability. Package of 6 x 4 mL. Shall contain bilirubin in the elevated neonatal range and the following analytes: Bilirubin (Direct), Calcium, Phenylalanine, Bilirubin (Indirect), Chloride, Potassium Bilirubin (Neonatal), Glucose, Sodium Caffeine, Magnesium, Theophylline 6. Liquichek Immunoassay Plus Level 1(Product No. 361) or equivalent: Human serum use. Shall have 14 day open vial stability at 2-8C except Folate which shall have 7 day stability. Package of 12 x 5 mL. Shall have the following analytes: Acetaminophen, hCG-Beta, Phenytoin, Testosterone AFP, Imipramine, Phenytoin (Free), Theophylline Amikacin, IgA, Procainamide, Tobramycin, Amitriptyline, IgE, Progesterone, TSH, Caffeine, IgG, Prolactin, Valproic Acid, Carbamazepine, IgM, PSA, Vancomycin, Digoxin, Lithium, T3 (Free), CEA, Iron, PSA (Free), Vitamin, B12, Cortisol, LH, Salicylate, Desipramine, Lidocaine, SHBG, Ferritin, NAPA, T3 (Total), Folate, Nortriptyline, T4 (Free), FSH, Phenobarbital, T4 (Total), Gentamicin 7. Liquichek Immunoassay Plus Level 3(Product No. 363) or equivalent: Human serum based, liquid, ready to use. Shall have 14 day open vial stability at 2-8C except Folate which shall have 7 day stability. Package of 12 x 5 mL. Shall have the following analytes: Acetaminophen, hCG-Beta, Phenytoin, Testosterone AFP, Imipramine, Phenytoin (Free), Theophylline, Amikacin, IgA, Procainamide, Tobramycin, Amitriptyline, IgE, Progesterone, TSH, Caffeine, IgG, Prolactin, Valproic Acid, Carbamazepine, IgM, PSA, Vancomycin, Digoxin, Lithium, T3 (Free), CEA, Iron, PSA (Free), Vitamin, B12, Cortisol, LH, Salicylate, Desipramine, Lidocaine, SHBG, Ferritin, NAPA, T3 (Total), Folate, Nortriptyline, T4 (Free), FSH, Phenobarbital, T4 (Total), Gentamicin 8. Liquichek Specialty Immunoassay Level 1(Product No. 364) or equivalent: Human serum based, liquid, ready to use. Shall have 30 day open vial stability at 2-8C for Intact PTH. Package of 6 x 5 mL. Shall have the following analytes: Anti-Tg, Erythropoietin, 25-Hydroxy Vitamin D Anti-TPO, Insuline Growth Factor, Osteocalcin, C-Peptide, Intact PTH 9. Liquichek Specialty Immunoassay Level 3(Product No. 366) or equivalent: Human serum based, liquid, ready to use. Shall have 30 day open vial stability at 2-8C for Intact PTH. Package of 6 x 5 mL. Shall have the following analytes: Anti-Tg, Erythropoietin, 25-Hydroxy Vitamin D Anti-TPO, Insuline Growth Factor, Osteocalcin, C-Peptide, Intact PTH 10. Lyphochek Quantitative Urine Control Level 1, Normal (Product No. 376) or equivalent: Shall be human urine based. Shall have 28 month shelf life at 2-8C. Package 12 x 10 mL. Shall contain the following analytes: 3-Methoxytyramine, Cystine, Phosphorus, Dopamine, Potassium, 11-B-Hydroxy-Etiocholanolone, 5-Aminolevulinic Acid (ALA) Dehydroepiandrosterone Porphyrins (Total) 5-HIAA, Epinephrine, 11-B-Hydroxy-Androsterone Estriol (Total) Pregnanetriol 11-Ketoetiocholanolone Etiocholanolone, Protein (Total), 11-Ketoandrosterone, Pregnancy (Qual), Glucose, Sodium, 17-Hydroxycorticosteroids, HVA, Specific Gravity 17-Ketosteroids, Hydroxyproline (Free), Urea, 17-Ketogenic Steroids, Hydroxyproline (Total), Urea Nitrogen Aldosterone, Iron, Uric Acid, AMP (Cyclic), Lead, Uroporphyrins, Androsterone, Magnesium, VMA, Arsenic, Mercury, Zinc, Barbiturate, Metanephrine, Creatinine, Calcium, Metanephrine (Total), Chloride, Microalbumin, Copper, Norepinephrine, Coproporphyrin, Cortisol, Osmolality, Normetanephrine, Creatine, pH 11. Lyphochek Quantitative Urine Control Level 2, Normal (Product No. 377) or equivalent: Shall be human urine based. Shall have 28 month shelf life at 2-8C. Package 12 x 10 mL. Shall contain the following analytes: 3-Methoxytyramine, Cystine, Phosphorus, Dopamine, Potassium, 11-B-Hydroxy-Etiocholanolone, 5-Aminolevulinic Acid (ALA) Dehydroepiandrosterone Porphyrins (Total) 5-HIAA, Epinephrine, 11-B-Hydroxy-Androsterone Estriol (Total) Pregnanetriol 11-Ketoetiocholanolone Etiocholanolone, Protein (Total), 11-Ketoandrosterone, Pregnancy (Qual), Glucose, Sodium, 17-Hydroxycorticosteroids, HVA, Specific Gravity 17-Ketosteroids, Hydroxyproline (Free), Urea, 17-Ketogenic Steroids, Hydroxyproline (Total), Urea Nitrogen Aldosterone, Iron, Uric Acid, AMP (Cyclic), Lead, Uroporphyrins, Androsterone, Magnesium, VMA, Arsenic, Mercury, Zinc, Barbiturate, Metanephrine, Creatinine, Calcium, Metanephrine (Total), Chloride, Microalbumin, Copper, Norepinephrine, Coproporphyrin, Cortisol, Osmolality, Normetanephrine, Creatine, pH 12. Liquichek Serum Volatiles Control Level 1(Product No. 383) or equivalent: Shall be human serum based. Shall have 10 day open vial-stability at 2-8C. Shall have 3 year shelf life at 2-8C. Package 6 x 5mL. Shall contain the following analytes; Acetone, Ethylene Glycol, Methanol (Methy Alcohol), Ethanol, Isopropanol (Isopropyl Alcohol) 13. Liquichek Serum Volatiles Control Level 2(Product No. 384) or equivalent: Shall be Shall be human serum based. Shall have 10 day open vial-stability at 2-8C. Shall have 3 year shelf life at 2-8C. Package 6 x 5mL. Shall contain the following analytes; Acetone, Ethylene Glycol, Methanol (Methy Alcohol), Ethanol, Isopropanol (Isopropyl Alcohol) 14. Liquichek Urine Chemistry Control Level 1(Product No. 397) or equivalent: Shall be human urine based, liquid, ready to use. Shall have at least 30 day open vial stability at 2-8C. Package of 12 x 10 mL. Shall contain the following analytes: Amylase, Microalbumin, Sodium Calcium, Osmolality, Specific Gravity Chloride, pH, Urea, Protein (Total), Cortisol, Phosphorus, Urea Nitrogen, Creatinine, Potassium, Magnesium, Uric Acid, Glucose, Pregnancy (Qualitative) 15. Liquichek Urine Chemistry Control Level 2(Product No. 398) or equivalent: Shall be human urine based, liquid, ready to use. Shall have at least 30 day open vial stability at 2-8C. Package of 12 x 10 mL. Shall contain the following analytes: Amylase, Microalbumin, Sodium Calcium, Osmolality, Specific Gravity Chloride, pH, Urea, Protein (Total), Cortisol, Phosphorus, Urea Nitrogen, Creatinine, Potassium, Magnesium, Uric Acid, Glucose, Pregancy (Qualitative) 16. Lyphochek Urine Metal Control Level 1 (Product No. 400) or equivalent: Shall be human urine based. Shall have 5 day reconstituted stability at 2-8C. Shall have 3 year shelf life at 2-8C. Package 10 x 25 mL. Shall contain the following analytes: 5-Aminolevulinic Acid (ALA), Copper, Mercury, Pentachlorophenol, Aluminum, Fluoride, Nickel, Antimony, Hippuric Acid, Arsenic, Lead, Phenol, Cadmium, Magnesium, Phenylglyoxylic Acid, Chromium, Mandelic Acid, Selenium, Cobalt, Manganese, Thallium, Trichloroacetic Acid, Zinc 17. Lyphochek Urine Metal Control Level 2 (Product No. 405) or equivalent: Shall be human urine based. Shall have 5 day reconstituted stability at 2-8C. Shall have 3 year shelf life at 2-8C. Package 10 x 25 mL. Shall contain the following analytes: 5-Aminolevulinic Acid (ALA), Copper, Mercury, Pentachlorophenol, Aluminum, Fluoride, Nicke, Antimony, Hippuric Acid, Arsenic, Lead, Phenol, Cadmium, Magnesium, Phenylglyoxylic Acid, Chromium, Mandelic Acid, Selenium, Cobalt, Manganese, Thallium, Trichloroacetic Acid, Zinc 18. Lyphochek Urine Bone Marker Control Bilevel (Product No. 406) or equivalent: Shall be human urine based. Shall have 5 day reconstituted stability at 2-8C. Shall have 3 year shelf life at 2-8C. Package 6 x 2 mL (3 of each level). Shall contain the following analytes: B-2-Microglobulin, Deoxypyridinoline (DPD), Pyridinoline (PYD), C-Telopeptide (CTx), N-Telopeptide (NTx), Creatinine, Pyridinium Corsslinks (DPD + PYD) 19. Lyphochek Whole Blood Metals Control Level 1 (Product No. 527) or equivalent: Shall be human whole blood based. Shall have 14 day reconstituted stability at 2-8C. Shall have at least 3 year shelf life at 2-8C. Package 6 x 2 mL. Shall contain the following analytes: Arsenic, Cadmium, Mercury, Lead, Thallium 20. Lyphochek Whole Blood Metals Control Level 2 (Product No. 528) or equivalent: Shall be human whole blood based. Shall have 14 day reconstituted stability at 2-8C. Shall have at least 3 year shelf life at 2-8C. Package 6 x 2 mL. Shall contain the following analytes: Arsenic, Cadmium, Mercury, Lead, Thallium 21. Lyphochek Whole Blood Metals Control Level 3 (Product No. 529) or equivalent: Shall be human whole blood based. Shall have 14 day reconstituted stability at 2-8C. Shall have at least 3 year shelf life at 2-8C. Package 6 x 2 mL. Shall contain the following analytes: Arsenic, Cadmium, Mercury, Lead, Thallium 22. Liquichek Ethanol/Ammonia Control Level 1(Product No. 544) or equivalent: Shall be liquid, ready to use. Ammonia concentration in level 1 must be within the normal reference range. Shall have at least a 2 year shelf life and 20 day open vial stability at 2-8C. Package of 6 x 3 mL. Shall have the following analytes: Ammonia, Ethanol 23. Liquichek Ethanol/Ammonia Control Level 3(Product No. 546) or equivalent: Shall be liquid, ready to use. Ammonia concentration in level 1 must be within the normal reference range. Shall have at least a 2 year shelf life and 20 day open vial stability at 2-8C . Package of 6 x 3 mL. Shall have the following analytes: Ammonia, Ethanol 24. Liquichek Tumor Marker Level 1(Product No. 547) or equivalent: Human serum based, liquid, ready to use. Shall have 30 day open vial stability at 2-8C for most analytes. Package of 6 x 2 mL. Shall have the following analytes: AFP, Ferritin, PSA, CA 15-3, hCG, PSA (Free), CA 19-9, hCG-Beta Subunit, Thyroglobulin, CEA, Prolactin, CA 27.29, IGF-1, CA 125, PAP 25. Liquichek Tumor Marker Level 2(Product No. 548) or equivalent: Human serum based, liquid, ready to use. Shall have 30 day open vial stability at 2-8C for most analytes. Package of 6 x 2 mL. Shall have the following analytes: AFP, Ferritin, PSA, CA 15-3, hCG, PSA (Free), CA 19-9, hCG-Beta Subunit, Thyroglobulin, CEA, Prolactin, CA 27.29, IGF-1, CA 125, PAP 26. Liquichek Tumor Marker Level 3(Product No. 549) or equivalent: Human serum based, liquid, ready to use. Shall have 30 day open vial stability at 2-8C for most analytes. Package of 6 x 2 mL. Shall have the following analytes: AFP, Ferritin, PSA, CA 15-3, hCG, PSA (Free), CA 19-9, hCG-Beta Subunit, Thyroglobulin, CEA, Prolactin, CA 27.29, IGF-1, CA 125, PAP 27. Liquichek Immunology Control Level 1(Product No. 594) or equivalent: Shall be human serum based, liquid and ready to use. Shall have at least 30 day open vial stability at 2-8C. Package of 6 x 3 mL. Shall contain the following analytes: Albumin, Complement C3, IgM, Apolipoprotein B, IgE, Rheumatoid Factor, Ceruloplasmin, IgG, Alpha-1-Antitrypsin Complement C4 Kappa Light Chain Antistreptolysin O, CRP, Lambda, IgA, Light Chain Antithrombin III, Haptoglobin, Prealbumin Apolipoprotein A-1, Protein (Total), Transferrin 28. Liquichek Immunology Control Level 3(Product No. 596) or equivalent: Shall be human serum based, liquid and ready to use. Shall have at least 30 day open vial stability at 2-8C. Package of 6 x 3 mL. Shall contain the following analytes: Albumin, Complement C3, IgM, Apolipoprotein B, IgE, Rheumatoid Factor, Ceruloplasmin, IgG, Alpha-1-Antitrypsin Complement C4 Kappa Light Chain Antistreptolysin O, CRP, Lambda, IgA, Light Chain Antithrombin III, Haptoglobin, Prealbumin Apolipoprotein A-1, Protein (Total), Transferrin 29. Multiqual Level 1(Product No. 697) or equivalent: Human serum based, liquid, ready to use. Shall have 30 day unopened stability at 2-8C. Shall have 14 day open vial stability at 2-8C. Shall have low osmolality value in level 1. Package of 12 x 10 mL. Shall have the following analytes: Acid Phosphatase, Calcium (Total), Glucose, Potassium Albumin, Carbon, UIBC, Sodium, Dioxide, TIBC, Protein (Total), Alkaline Phosphatase, Chloride, Phosphorus Bilirubin (Total), ALT, Cholesterol (HDL), LDH, Triglycerides, Amylase, Iron, Bilirubin (Direct), Creatinine, Osmolality, Cholesterol (LDL), Lactic Acid, Urea, Nitrogen, Amylase (Pancreatic), Cholesterol (Total), GGT, Lipase, Uric Acid, AST, Cholinesterase, Magnesium, Bilirubin (Neonatal), CK 30. Multiqual Level 3 (Product No. 699) or equivalent: Human serum based, liquid, ready to use. Shall have 30 day unopened stability at 2-8C. Shall have 14 day open vial stability at 2-8C. Shall have low osmolality value in level 1. Package of 12 x 10 mL. Shall have the following analytes: Acid Phosphatase, Calcium (Total), Glucose, Potassium Albumin, Carbon, UIBC, Sodium, Dioxide, TIBC, Protein (Total), Alkaline Phosphatase, Chloride, Phosphorus Bilirubin (Total), ALT, Cholesterol (HDL), LDH, Triglycerides, Amylase, Iron, Bilirubin (Direct), Creatinine, Osmolality, Cholesterol (LDL), Lactic Acid, Urea, Nitrogen, Amylase (Pancreatic), Cholesterol (Total), GGT, Lipase, Uric Acid, AST, Cholinesterase, Magnesium, Bilirubin (Neonatal), CK 31. Liquichek Spinal Fluid Control Level 1(Product No. 751) or equivalent: Shall be human based, liquid and ready to use. Shall have at least 30 day open vial stability at 2-8C. Package of 6 x 3 mL. Shall contain the following analytes: Albumin, IgG, Protein electrophoresis, Chloride, IgM, Protein (Total), Glucose, Lactate, Sodium, IgA, LDH 32. Liquichek Spinal Fluid Control Level 2(Product No. 752) or equivalent: Shall be human based, liquid and ready to use. Shall have at least 30 day open vial stability at 2-8C. Package of 6 x 3 mL. Shall contain the following analytes: Albumin, IgG, Protein electrophoresis, Chloride, IgM, Protein (Total), Glucose, Lactate, Sodium, IgA, LDH 33. Lyphochek Whole Blood Level 1, 6x2mL (Product No. 274) or equivalent: 34. Lyphochek Whole Blood Level 3, 6x2mL (Product No. 276) or equivalent: 35. Lyphochek Whole Blood Level 4, 6x2mL (Product No. 277) or equivalent: 36. Liquichek Assayed Multiqual Premium (Product No. 284) or equivalent: 37. Liquichek Assayed Multiqual Premium (Product No. 286) or equivalent: 38. TDM QC Level 1, 12x5mL (Product No. 725) or equivalent: 39. TDM QC Level 2, 12x5mL (Product No. 726) or equivalent: 40. TDM QC Level 3, 12x5mL (Product No. 727) or equivalent: 41. Utox QC S1E Low Opiate, 10x10mL (Product No. 423) or equivalent: 42. Utox QC S2E Low Opiate, 10x10 mL (Product No. 424) or equivalent: 43. Utox QC Negative, 10x20 mL (Product No. 460) or equivalent: 44. Unity Real Time Annual Subscription 45. Connectivity Support Annual Subscription 46. Unity Real Time Additional Database This is not a solicitation. This information is for planning purposes only and is not to be construed as a commitment by the Government, implied or otherwise, to issue a solicitation or award a contract. Vendors responding to this sources sought notice are advised their response does not ensure participation in future solicitations or contract awards. The Government will not reimburse any company or individual for any expense associated with preparation or participation in this research. Interested parties should e-mail responses to contact@example.gov by the date identified below. Hard copies of the responses are not required and will not be accepted. Vendor responses should include: 1. The size of your business with regard to North American Industry Classification System (NAICS) code 325413 per the standard described in Federal Acquisition Regulation (FAR) Part 19.102 (FAR available at https://acquisition.gov). 2. Company name, DUNS, CAGE, Contact information including phone number and email. 3. Specifically identify whether your company is capable of providing immunoassay control kits to include all supplies listed above. 4. Submit your response no later than 26 July 2019 by 12:00 noon CST.