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This Sources Sought opportunity was posted on August 3, 2018. The submission period has ended. Browse the details below for market research, or find similar active opportunities.

Sexually Transmitted Disease Reagents, Consumables, Testing, Service and Maintenance

Closed
W81K00-18-T-M078Federal

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
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

1 day ago

DEADLINE

in 24 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

2 days ago

DEADLINE

in 13 days

General Info

Agency

N/A

NAICS

325413 - In-Vitro Diagnostic Substance Manufacturing

Place of Performance

Evans Army Community Hospital, Fort Carson, CO, 89013, USA

Set-Aside

NONE

Documents

0

No documents available

Documents will appear here when they are available.

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Uniform Contract Format

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Timeline

PhaseClosed
Posted

Sources Sought

Response Deadline

Deadline has passed

Submission Closed

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Organization & Contact Information

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AgencyN/A
Contacts2 people available
OfficeN/A
Organization / Agency
N/A
Office AddressN/A
Contacts
Joseph Mitchell BrownContract Specialist
Troy DavisContracting Officer

Full Description

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SOURCES SOUGHT NOTIFICATION The US Army Medical Command, Regional Health Contracting Office-Central, Fort Carson Health Contracting Cell is issuing this sources sought for market research purposes only. Any responses to this notice will be used for planning purposes only. This is not a solicitation of offers, nor is it a notice to proceed. Evans Army Community Hospital (EACH) has a requirement for Sexually Transmitted Disease testing utilizing a multi-test single platform compatible with ThinPrep specimen collection. The required testing includes: a. Chlamydia trachomatis (CT) and Neisseria gonorrhea (NG) combination: 13,000 tests annually. b. Human Papilloma Virus (HPV): 7,000 tests annually. Contractor must be able to provide all reagents and consumables for a high throughput analyzer with an estimate of 20,000 samples per year. Contractor must be able to perform bi- annual calibrations and/or preventive measures at no cost to the government. Contractor must be available to perform emergencyservices within 24 hours of service call and be completed within 48 hours of arrival at no cost to the government. A. The contractor shall provide one (1) system to perform the following tests: - Chlamydia trachomatis - Neisseria gonorrhea - Human Papillomavirus B. The specifications for the Human Papillomavirus and Chlamydia trachomatis/Neisseria gonorrhea analyzer that we are requesting are as follows: - Must be capable of processing 250 samples in an 8 hour shift. - Must have FDA approved assays and reagents - System must be compatible with current Aptima urine collection kit and thin prep collection method. - Must be automated sample preparation, amplification and detection. - Must possess Liquid Level detection capability to confirm adequate sample and reagent levels. - Data Management system shall (must) have a user friendly "Windows Based" interface that shall include a data management system for operational control of the analyzer system, management of the QC program, on-instrument useful life of the reagents/reagent packs, and management of patient results. - Must be able to process Urine, Swab and Thin Prep specimens. - Must be capable of automatically sending patient results to a Laboratory Information System (LIS). - Must come equipped with an un-interruptible power supply capable of providing all necessary electrical power to the analyzer system, to include the data management system, for 15 to 20 minutes. - Complete system dimensions must be no greater than 50(W)x40(D)x70(H) in inches - Analyzer computer workstation dimensions must be no greater than 33x36 inches - Must give results no more than 3.5 hours from start of run - Waste must drain directly to removable collection containers THERE IS NO SOLICITATION AT THIS TIME. This sources sought is issued solely for information and planning purposes - it does not constitute a Request for Proposal (RFP) or a promise to issue an RFP in the future. This sources sought and request for information does not commit the Government to contract for any supply or service whatsoever. The government is not at this time seeking proposals and will not accept unsolicited proposals. Proprietary information, if any, should be minimized and MUST BE CLEARLY MARKED. To aid the Government, please segregate proprietary information. Please be advised that all submissions become Government property and will not be returned. Vendors that consider themselves capable of providing the required testing are invited to submit a capability statement for the Government to consider via email to the Point of Contact listed herein. The capability statement shall include the following: 1. Vendor name (to include CAGE code and DUNS number); Point of Contact (to include e-mail address and hone number); business size. 2. Documentation that demonstrates the capability of equipment to perform all tests listed above. This documentation shall include information such as, but not limited to: a. Food and Drug Administration approval; b. Platform physical characteristics (e.g., dimensions, sample/specimen handling capacity per hour, ThinPrep sample collection compatible); and, c. Timeline for installation of equipment upon receipt of an official award, including calibrations or verification process. Telephone inquiries will not be accepted or acknowledged, and no feedback or evaluations will be provided to companies regarding their submissions. Submission Instructions: August 10, 2018, 10:00 am Mountain Daylight Time. All responses to or questions concerning this Sources Sought Notice must be emailed to the Contract Specialist, Joseph (M) Mitchell Brown at joseph.m.brown250.civ@mail.mil. Interested sources are invited to submit a response to this Sources Sought Notice by August 10, 2018, 10:00 am Mountain Daylight Time. All responses to or questions concerning this Sources Sought Notice must be emailed to the Contract Specialist, Joseph (M) Mitchell Brown at joseph.m.brown250.civ@mail.mil.

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