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This Government Contract opportunity from Department Of Veterans Affairs was posted on July 31, 2024. The submission period has ended. Browse the details below for market research, or find similar active opportunities.

6550--Lab Supplies - (Cepheid Gene Expert Lab Test Kits) - VISN New Requirement (5-Year) - VISN 04

Closed
36C24424Q0803Federal

Contract Overview

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

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NAICS: 325413
New
Federal
Cost Per Reportable Result Purchase of Immunohistochemistry Reagents for Laboratory Tests.
Solicitation # 36C26027Q0058
The Department of Veterans Affairs, through Network Contracting Office 20, is seeking a comprehensive histology staining workflow system for the Puget Sound Health Care System in Seattle, Washington. The required system must include two immunohistochemistry and two in-situ hybridization immunostainers, two special stainers, and an integrated specimen tracking system to ensure patient safety, maintain a chain of custody, and monitor productivity. The workflow components must be fully automated, communicate with one another, and maintain compatibility with Data Innovations middleware as well as VISTA, Cerner, and any future electronic health record systems acquired by the VA. The contract follows a Cost Per Reportable Result pricing model and spans a base year from February 1, 2027, to January 31, 2028, with four subsequent one-year option periods extending through January 31, 2032. Technical requirements specify that the immunostainers must perform 100% of tests listed in the provided specifications and support simultaneous IHC, ISH, and Direct Immunofluorescence staining. Equipment must support Code 39 and Code 128 barcodes, include a safe hazardous waste removal system, and be provided with an uninterruptible power supply capable of supporting a 15-minute controlled shutdown. The contractor is responsible for the delivery, installation, and removal of equipment at no additional charge and must guarantee a minimum equipment uptime of 98%. Performance and method validation must adhere to CLSI guidelines and College of American Pathologists standards. Additionally, the contractor must comply with strict federal and VA information security directives, including those regarding data confidentiality and media sanitization. Emergency supply orders must be fulfilled within 24 hours of a verbal request, providing enough consumables for one week of normal operation.
260-NETWORK Contract Office 20 (36C260)

POSTED

2 days ago

DEADLINE

in 23 days
NAICS: 325413
New
Federal
6550--HEMOCHRON SIGNATURE ELITE REAGENTS AND SUPPLIES
Solicitation # 36C26227Q0046
The Department of Veterans Affairs, Network Contracting Office 22, is conducting a sources sought notice for the procurement of FDA approved reagents, supplies, consumables, and quality control materials for Werfen Hemochron Signature Elite instruments. This requirement supports the Pathology and Laboratory Medicine Service at the Southern Arizona VA Health Care System in Tucson, Arizona. The contract structure includes a base year from January 1, 2027, to December 31, 2028, followed by four subsequent option years extending through December 31, 2032. The selected contractor must provide 24/7 technical and product support at no additional cost and ensure all items are fully compatible with existing instrumentation without requiring workflow changes or retraining. Key operational requirements include strict adherence to manufacturer specifications for packaging and temperature control during transport. All supplied materials must maintain a minimum shelf life of 90 days, and shipments must clearly list lot numbers and expiration dates. Standard orders are required to be delivered within four working days, while emergency deliveries for defective or temperature-compromised items must be completed within 24 hours of a verbal order. This procurement is conducted as a brand name or equal acquisition under FAR 52.211-6. Interested respondents must provide their business size status, SAM.gov identifiers, and evidence of compliance with the Buy American Act and the Non-Manufacturer Rule.
262-NETWORK Contract Office 22 (36C262)

POSTED

3 days ago

DEADLINE

in 12 days

General Info

NAICS

325413 - In-Vitro Diagnostic Substance Manufacturing

Place of Performance

PA

Set-Aside

NONE

Documents

2

36C24424Q0803 - Lab Supplies (Cepheid Gene Expert Lab Test Kits) - VISN 04

DOCX, High priority: read this firstsources-sought
High

Table of Deliverables/Consumables - Cepheid 24-25

DOCX, High priority: read this firstspecifications
High

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Timeline

1 update
PhaseClosed
Response Deadline

Deadline has passed

Posted

special-notice

Notice updated

Response deadline changed from Jul 7, 2024 to Aug 2, 2024. Set-aside added: 8(a) Sole Source. The notice description changed. The point of contact changed.

Submission Closed

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Organization & Contact Information

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AgencyDepartment Of Veterans Affairs → 244-NETWORK Contract Office 4 (36C244)
Contacts1 person available
OfficePITTSBURGH, PA, 15215, USA
Office AddressPITTSBURGH, PA, 15215, USA
Contacts
Yazmin AlvarezContract Specialist

Full Description

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INTENT TO SOLE SOURCE Department of Veterans Affairs (VA), VISN 04, Altoona VA Medical Center hereby gives notice of the Government s intent to establish a single award fixed price Indefinite Delivery/ Indefinite Quantity (IDIQ) contract for a period of performance of 5 years with Cepheid: 904 Caribbean Dr., Sunnyvale, CA 94089-1189 to acquire Cepheid GeneXpert Test Kits and Supplies. This IDIQ will be used as a simplified method of filling anticipated repetitive needs of laboratory reagents and supplies at the participating duty stations: Altoona VA Medical Center, 2907 Pleasant Valley Boulevard, Altoona, PA 16602-4377, United States. VA Butler Healthcare, 325 New Castle Road, Butler, PA 16001-1138, United States. Coatesville VA Medical Center, 1400 Black Horse Hill Road, Coatesville, PA 19320-2096, United States. Erie VA Medical Center, 135 East 38th Street, Erie, PA 16504-1559, United States. Lebanon VA Medical Center, 1700 South Lincoln Avenue, Lebanon, PA 17042-7529, United States. Philadelphia VA Medical Center, 3900 Woodland Avenue, Philadelphia, PA 19104-4551, United States. VA Pittsburgh Healthcare System, University Drive Campus, University Drive C, Pittsburgh, PA 15240- 1003, United States. VA Pittsburgh Healthcare System, HJ Heinz Campus, 1010 Delafield Road, Pittsburgh, PA 15215-1802, United States. Wilkes-Barre VA Medical Center, 1111 East End Boulevard, Wilkes-Barre, PA 18711-0026, United States. Wilmington VA Medical Center, 1601 Kirkwood Highway, Wilmington, DE 19805-4917, United States. This IDIQ will be established with a single source, Cepheid, because they are the sole manufacturer of the required reagents, kits, and supplies for the GeneXpert Infinity analyzer. Determination of this single source procurement is in accordance with Only One Responsible Source and No Other Supplies or Services Will Satisfy Agency Requirements per 41 USC §3304(a)(1) as implemented by FAR 6.302-1. It is the Government s belief that the proposed candidate is the only provider of the reagents, kits, supplies, and service that are compatible with the GeneXpert Infinity analyzer that can meet the agency s needs. The applicable North American Industry Classification System (NAICS) code is 325413 (In-Vitro Diagnostic Substance Manufacturing) and the Product Service Code (PSC) is 6550 (In Vitro Diagnostic Substances, Reagents, Test Kits and Sets). This notice of intent is not a request for competitive quotes. Telephone requests will not be accepted. However, any business that believes it can provide Cepheid GeneXpert Infinity Molecular Reagents and Supplies may give written notice to yazmin.alvarez@va.gov by 2:00PM Eastern Time on July 7, 2024. Supporting evidence must be furnished in sufficient detail to demonstrate the ability to comply with the requirement. Responses will be considered by the Government; however, a determination by the Government not to compete the proposed acquisition based upon responses of this notice is solely within the discretion of the Government. THIS SYNOPSIS DOES NOT COMMIT THE GOVERNMENT TO CONTRACT FOR ANY SUPPLY OR SERVICE. THE GOVERNMENT WILL NOT PAY FOR ANY INFORMATION OR ADMINISTRATIVE COSTS INCURRED IN RESPONSE TO THIS SYNOPSIS. Statement of Work Cost Per Reportable Test Reagent Rental Agreement for Cepheid GeneXpert Instruments, Laboratory Reagents, Controls, and Supplies 1. Purpose Requesting Base period of twelve (12) months plus four (4) additional options of 12 Months (Base Period from September 21, 2024, through September 20, 2025). Cost Per Reportable Test Reagent Rental Agreement for Cepheid GeneXpert Instruments, Laboratory Reagents, Controls and Supplies for C. diff, CT/NG, MTB, MRSA SKIN, CARBA-R, MRSA, STREP A, NOROVIRUS, FLU A, FLU B, RSV, SARS-COV-2, and MVP testing. Current contract number is 36C24421D0130, which is only for reagents. Would like to combine contract to reflect these additional test and instruments. 2. Scope Below is a list of items that the vendor will provide as an agreement in the cost per reportable test reagent rental agreement for Cepheid GeneXpert instruments, Laboratory Reagents, Controls, and Supplies. Vendor will remove current GeneXpert analyzers and replace it with new GeneXpert analyzers which are to be used in VISN 4 facilities. Vendor will provide maintenance for new instruments at the defined recommendations of the manufacturer and provide technical support 24/7. Vendor will provide all necessary Cepheid GeneXpert Laboratory Test Kits and supplies as needed to perform C. diff, CT/NG, MTB, MRSA SKIN, CARBA-R, MRSA, STREP A, NOROVIRUS, FLU A, FLU B, RSV, SARS-COV-2, and MVP testing. Should during the rental of this instrument, another version is released, Pathology and Laboratory Medicine Service in VISN 4 has the right to change to the most recent and updated version should they desire to do so. Vendor will also sponsor and provide training courses for instrumentation. Vendor will provide a warranty on the instrument that will start once instruments are installed and additional warranty service if needed. Vendor will provide initial setup that includes verification/validation of the instrument and any additional technical service during the initial phase of the rental. Testing is cleared by the FDA for in-vitro diagnostic use and is CLIA Moderately Complex Testing. Technical assistance and information will be offered on how to best meet the IQCP process. 3. Location These supplies will be used on the Cepheid GeneXpert Analyzers for the following locations in VISN 4: Duty Station 1: Altoona VA Medical Center, 2907 Pleasant Valley Boulevard, Altoona, PA 16602- 4377, United States. Duty Station 2: VA Butler Healthcare, 325 New Castle Road, Butler, PA 16001-1138, United States. Duty Station 3: Coatesville VA Medical Center, 1400 Black Horse Hill Road, Coatesville, PA 19320- 2096, United States. Duty Station 4: Erie VA Medical Center, 135 East 38th Street, Erie, PA 16504-1559, United States. Duty Station 5: Lebanon VA Medical Center, 1700 South Lincoln Avenue, Lebanon, PA 17042-7529, United States. Duty Station 6: Philadelphia VA Medical Center, 3900 Woodland Avenue, Philadelphia, PA 19104- 4551, United States. Duty Station 7A: VA Pittsburgh Healthcare System, University Drive Campus, University Drive C, Pittsburgh, PA 15240-1003, United States. Duty Station 7B: VA Pittsburgh Healthcare System, HJ Heinz Campus, 1010 Delafield Road, Pittsburgh, PA 15215-1802, United States. Duty Station 8: Wilkes-Barre VA Medical Center, 1111 East End Boulevard, Wilkes-Barre, PA 18711-0026, United States. Duty Station 9: Wilmington VA Medical Center, 1601 Kirkwood Highway, Wilmington, DE 19805- 4917, United States. 4. Performance Requirements: Maintenance: The Vendor shall perform preventive maintenance at intervals specified by the manufacturer to ensure proper equipment performance. Maintenance includes the following: 4.1.1 Inventory and recording of systems components. 4.1.2 Monthly deliverables shall be received in full. 4.1.3 Test all components for proper test performance. Equipment shall reproduce results according to manufacturer s specifications. 4.1.4 After Preventative Maintenance (PM), the vendor shall submit a detailed work report to the COR for notice at no additional cost to the government. 4.1.5 Delivery of PM parts or material. The vendor shall provide all preventive service materials at no additional cost the government. 4.2. On-call Repairs: On-call repairs are emergency repairs beyond the scheduled maintenance. 4.2.1 The vendor shall provide technical assistance not limited to test performance, or equipment malfunction twenty-four (24) hours a day, seven (7) days a week, including all Federal and religious holidays, via direct communication thru a telephone bank with technically capacitated and certified personnel by the vendor. 4.2.2. The vendor shall respond to a call for on-site repair and be at the job site within two (2) hours during regular working hours, Monday Friday, 0800 16:00 hours. In very urgent cases, an immediate repair can be requested after 1600 hours and on Saturdays, Sundays, and Federal holidays. After repair, the vendor shall submit a detailed work report to include all required materials and is to be at no-charge to the facility. 4.2.3. If the problem cannot be resolved over the phone the vendor will have a service technician dispatched immediately to resolve the problem. Vendor will agree that if the instrument is a rental agreement and should there be ongoing and/or adverse operating issues with the instrument within the year of purchase, the vendor will work to resolves these problems. If the problems cannot be resolved, vendor agrees to either replace the instrument if customer agrees or void the rental agreement. 4.2.2.2 If the malfunction is reported to the vendor not later than 1600 hours, the failure elimination shall be started immediately on the same day. 4.3. For delivery of repairs parts or materials the vendor shall provide all parts and materials at no additional cost the government. 4.3.1 Vendor shall remove all parts, equipment or materials replaced, or upgraded by the vendor due to and not limited to repairs, replacements, recall, and upgrades without any cost to the Government. 4.4 Safety 4.4.1 Vendor shall immediately notify the service of any changes in reagents kits composition, procedure modification, recall notification or any changes that will affect the performance of the test or procedure according to FDA regulations. 4.5 Test Performance 4.5.1 All test and procedures must comply and be approved by the FDA. 4.5.2. All test, procedures, and equipment must perform at manufacturer specifications, deviations from the performance specifications shall be corrected by the vendor. 4.5.3. All test performance will be evaluated by and not limited for performance thru peer comparison, quality control and CAP peer evaluation according to CLIA 5. Deliverables/Supplies This order is for the cost per test procurement of the GeneXpert instruments under the terms of the reagent rental agreement. (List of test and supplies are listed below in Table 1) 5.1 The vendor shall provide on-site training for new personnel (as required) for testing and procedures of aforementioned, offeror shall conduct instructional course(s) to meet the objectives identified in paragraph 4. In addition, the vendor shall provide handouts and training materials in sufficient quantity for each participant. These are off-the-shelf courses. The vendor shall provide lesson plan, course materials and media (DVD s, CD s, videos, etc. if required) for each procedure at no additional cost. 5.2 The vendor shall deliver all equipment and UPS necessary for test performance at no Government cost. 5.2.1 The vendor shall deliver all and not limited to operational, maintenance, troubleshooting, small repairs, equipment specifications and test manuals. 5.3 The vendor shall install the equipment and perform test verification according to manufacturer specification, CLIA, FDA and CAP requirements. 5.4 In the event that requested supplies are on back-order, vendor is to inform COR as to the estimated time of availability. 5.4.1 The items on this contract are not on a delivery schedule. Th customer will call vendor with order request for items needed. 5.5 The vendor shall deliver all invoices for review according to the established contract at the end of each billing cycle. 5.5.1 All items not contracted shall be specifically detailed on the invoice including description, quantity acquired, and government cost. 5.6 Remedies: 5.6.1 Any changes in reagents or equipment modifications shall be immediately disclosed by the vendor electronically as well as by postal mail with supporting documentation of the change and, detailed guidance against implementation within twenty-four hours of its application or according to FDA guidelines. 5.6.2 Additional charges incurred by the government to provide the continuity of contracted tests to patients and not limited to outsourcing, transportation and or any other additional cost shall be covered by the vendor at no additional charge to the government. TABLE 1 CLIN # TABLE OF DELIEVERABLE/CONSUMABLES 0001 REGULAR FLOCKEDSWAB W/UTM W/OBEADS 50PCS 0002 ESWAB,LIQUID AMIES, FLOCKED, COPAN,480CFA 0003 CEPHEID COLLECTION DEVICE (50) 0004 KIT,GX,10-TEST,EBOLA,EUA 0005 KIT,MPOX,10 TEST 0006 KIT,BCR-ABL ULTRA P 190,10-TESTS,GX,RUO 0007 KIT,NPM1 MUTATION,CRUO,GX,10-TEST 0008 SINGLE-USE DISPOSABLE SWAB - 120-COUNT 0009 A CASE OF CEPHEID COLLECTION DEVICE (500) 0010 COLLECTION KIT, XPERT SWAB, US IVD, 50 0011 CollectionKitA urine 0012 KIT,10-TEST,GBS,EXPRESS,US-IVD 0013 MINITIP FLOCKEDSWAB WUTM W/OBEADS 50PCS 0014 KIT,BCR-ABL UYLTRA,US-IVD,10-TEST 0015 KIT,XPRESS,STREPA,US-IVD,10 TEST 0016 KIT,XPRESS,MVP,US-IVD,10 TEST 0017 KIT,CARBA-R,IVD,GX 0018 KIT,CDIFF/EPI,GX,IVD,10-TEST 0019 KIT,CDIFF,10-TESTS,GX,IVD 0020 KIT,CT/NG,GX,IVD 0021 KIT,EV,10-TESTS,GX,IVD 0022 KIT,FII/FV,10-TESTS,GX,IVD 0023 KIT,10-TEST,GBS,LB,XC,US-IVD 0024 KIT,MRSA,10-TESTS,GX,IVD 0025 KIT,10-TEST,MRSA NXG,IVD,GX 0026 KIT,MRSA/SA BC,10-TESTS,GX,IVD 0027 KIT,MRSA/SA SSTI,10-TESTS,GX,IVD 0028 KIT,MTB,IVD,US 0029 KIT,GX,10-TEST,NOROVIRUS,US-IVD 0030 KIT,SA COMP,10-TESTS,GX,IVD 0031 KIT,XPERT TV_US,10-TEST 0032 KIT,VANA,10-TESTS,GX,US-IVD 0033 STARTER KIT,GX CARBA-R,IVD 0034 BUNDLE,OEM CONTROLS AND PANEL,CARBA-R,GX 0035 STARTER KIT, GX C. DIFFICILE/EPI, IVD 0036 BUNDLE,CDIFF/EPI CONTROLS AND PANEL 0037 CT/NG START PACK 0038 BUNDLE,OEM CONTROL REAGENTS,CT/NG 0039 START PAK FOR MRSA NXG ASSAY 0040 BUNDLE,MRSA NXG,CONTROLS 0041 GXMRSA/SA BC START PAK 0042 BUNDLE,OEM CONTROL REAGENTS,MRSA/SA 0043 START PAK FOR MRSA ASSAY 0044 BUNDLE,OEM CONTROL REAGENTS,MRSA/SA 0045 STARTPAK,MTB/RIF,PAIR WITH MTB/RIF-BU2 0046 BUNDLE,CONTROLS AND PANEL,MTB/RIF 0047 STARTPAK FOR XPERT TV PRODUCT 0048 TV CONTROLS AND PANEL BUNDLE 0049 STARTPAK,XPRS MVP 0050 BUNDLE,CONTROLS AND PANEL,XPRESS,MVP 0051 STARTPAK FOR XPRESS STREP A PRODUCT 0052 BUNDLE,CONTROLS AND PANEL,XPRESS,STREP A 0053 GBS, LB, XC, START PACK 0054 BUNDLE, GBS, LB, XC, CONTROLS 0055 XPRESS GBS START PACK 0056 BUNDLE,XPRESS GBS, CONTROLS 0057 FII/FV START PACK 0058 BUNDLE,OEM CONTROL REAGENTS,FIIFV

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