7H20--Automated Patient Label Printing and Tracking System
Contract Overview
Solicitation details, issuing organization, response deadlines, documents, and interested companies for this government contract opportunity.
AI Contract Overview
The contract solicitation 36C26126Q0864 seeks the LATTICE Automated Patient Label Printing and Tracking System to be deployed at the VA San Francisco Health Care System, with a base performance period from July 1, 2026, through June 30, 2027, and four one-year option years extending through June 30, 2031. The estimated total value is $47 million, covering the procurement of 45 ZQ610-HC mobile printers, corresponding five-year service plans, 5-slot charging cradles, a site license for 100 beds, and annual 24x7 support for five consecutive years. Delivery is FOB destination to the specified VA facility, with acceptance and inspection conducted on-site by the Government. The contract is structured as a commercial item acquisition under FAR Part 12, using a Firm Fixed Price (FFP) model, with award based on a trade-off between price and other factors, though specific non-price criteria and their weights are not detailed. The contracting officer is Tawnya Krommenhoek, and offers must be submitted via email by the deadline of June 25, 2026, at 10:00 a.m. MST. The contract imposes stringent compliance requirements through incorporated FAR clauses, including mandatory adherence to cybersecurity standards under 52.240-91 and 52.240-93, which mandate safeguarding of contractor information systems and prohibit certain security risks. It also requires compliance with anti-discrimination policies under 52.222-90 and prohibits contractors from requiring internal confidentiality agreements that restrict whistleblower rights. The contractor must validate small business status, provide UEI and CAGE codes, and disclose any involvement with entities in Sudan, Iran, or use of prohibited telecommunications equipment. Invoicing is strictly electronic via the Tungsten Network integrated with the VA’s EIPP system, and paper invoices are not accepted. Packaging and marking requirements emphasize accurate labeling with brand, model, and manufacturer identifiers, and barcode integrity for medical specimen tracking, though no specific military or industry standards are cited. No COR/COTR is named, and while the technical specifications for the system are not detailed in Section C, acceptance is contingent on the delivered system conforming to contractual requirements and applicable regulatory standards referenced in clause 852.211-72.
General Info
Timeline
Organization & Contact Information
Full Description
Lattice MediCopia is an Automated Positive Patient Identification System which collects laboratory specimens, including but not limited to, blood, urine, stool, swabs, and other biological and pathology samples. Lattice MediCopia is a specialized and proprietary solution that provides a robust, integrated mobile system paired with handheld computers and scanners for bedside collection, labeling, and printing.
The MediCopia Specimen Collection system is the only known VA Technical Reference Model (TRM) approved, fully compatible, automated bedside specimen collection solution capable of meeting the VA s mission critical requirements for Positive Patient Identification, barcode accuracy, and seamless interoperability with VA s Veterans Health Information System and Technology Architecture (VISTA), Computerized Patient Record System (CPRS), the Laboratory Information System, and existing VA standard hardware and software. There are no known alternative vendors or solutions which can provide a comparable system that meets all required security, privacy, and integration standards which include the National Institute of Standards and Technology (NIST), Federal Information Processing Standards (FIPS), Health Insurance Portability and Accountability Act (HIPAA), and VA Handbook 6500.
The specific items required are attached.
VA s Gray Market Items terms and conditions apply pursuant to VAAR 852.212-71 Gray Market Items and VAAR 852.212-72 Gray Market and Counterfeit Items. As a result, vendor shall be an OEM, authorized dealer, authorized distributor or authorized reseller for the items identified to be eligible for participation with this acquisition. Vendor must be able to provide the documentation that demonstrates such aforementioned authority. The solicitation for this action will be posted to beta.sam.gov and all responsible sources may submit a capability statement, proposal, or quotation, which shall be considered by the agency. After consideration, the Government will determine whether to proceed with the sole source acquisition. Please keep in mind that patient care and choice in the decision is the highest priority to the VA. The solicitation will be posted on or about June 23, 2026. Please respond to Tawnya Krommenhoek at contact@example.gov no later than Thursday, June 25, 2026 at 10:00 am Mountain Standard Time. With your response, please provide evidence showing compliance with the aforementioned Gray Market clauses. Failure to provide the required information may result in a determination that your company is not a viable source. (End of Notice)
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