SAM #36C25226Q0365

Sole Source Integration of Fujifilm PACS with Federal EHR at Jesse Brown VA Medical Center

This opportunity involves a sole source procurement by the Department of Veterans Affairs for integration services at the Jesse Brown VA Medical Center in Chicago, IL. - The Great Lakes Acquisition Center (GLAC) intends to award a contract to FujiFilm Healthcare Americas Corporation - Purpose: Integrate the existing Synapse/Sonosite Synchronicity PACS with the new Federal Electronic Health Record (FEHR), Oracle Health - Only FujiFilm, as the OEM, is authorized to provide this integration service - All products and services must be new OEM items; no used, refurbished, remanufactured, gray market, or counterfeit items are allowed - Vendors must be OEM authorized dealers, distributors, or resellers - All technical personnel must be OEM certified - NAICS code: 541519 (Other Computer Related Services) - No specific part numbers or quantities are listed; this is a one-time service contract - No competitive quotes are being solicited; this is a justification for sole source procurement - Place of performance: Jesse Brown VA Medical Center, Chicago, IL - Contracting office: Great Lakes Acquisition Center, Milwaukee, WI

Description

Under Statutory Authority 41 U.S.C. 1901 the VA Great Lakes Acquisition Center (GLAC) intends to negotiate a sole source contract with FujiFilm Healthcare Americas Corporation to integrate the existing Synapse/Sonosite Synchronicity point of care ultrasound picture Archiving and Communication System (PACS) with the new Federal Electronic Health Record (FEHR), Oracle Health, at the Jesse Brown VA Medical Center in Chicago, IL. This support is only authorized by the Original Equipment Manufacturer (OEM), FujiFilm Healthcare Americas Corporation.

This acquisition is conducted under the authority of 41 U.S.C. 1901 Simplified Acquisition Procedures as implemented in FAR 13.106-1(b)(1), only one responsible source and no other supplies or services will satisfy agency requirements. The NAICS Code is 541519.

This Notice of Intent is not a request for competitive quotes. No solicitation documents are available, and telephone requests will not be honored. However, if a firm believes it can meet the requirements it must furnish information about its products and services, as well as references from other customers who are using these products and services to the Contracting Officer by 10:00am CDT on 04/06/2026. Supporting evidence must be furnished in sufficient detail to demonstrate the ability to comply with the above requirements. This evidence shall include the following:

1.) A letter from the Original Equipment Manufacturer (OEM) stating vendor is an authorized distributor per clause 852.212-71(c). 2.) Proof vendor can purchase OEM parts, if required. 3.) Proof all technical personnel are OEM certified. 4.) Proof the firm can utilize OEM s billable service, if using.

Responses received will be evaluated, however; a determination by the Government not to compete the proposed procurement based upon responses to this notice is solely within the discretion of the Government. If no responses are received, the Contracting Officer will proceed with the sole source negotiation with FujiFilm Healthcare Americas Corporation.

Capability statements shall be submitted by email only as a MS Word or Adobe PDF attachment to Eileen Meyer at eileen.meyer@va.gov. TELEPHONIC INQUIRIES WILL NOT BE ACCEPTED.

VAAR 852.212-71 GRAY MARKET AND COUNTERFEIT ITEMS (FEB 2023) (a) No used, refurbished, or remanufactured supplies or equipment/parts shall be provided. This procurement is for new Original Equipment Manufacturer (OEM) items only. No gray market items shall be provided. Gray market items are OEM goods intentionally or unintentionally sold outside an authorized sales territory or sold by non-authorized dealers in an authorized sales territory. (b) No counterfeit supplies or equipment/parts shall be provided. Counterfeit items include unlawful or unauthorized reproductions, substitutions, or alterations that have been mismarked, misidentified, or otherwise misrepresented to be an authentic, unmodified item from the original manufacturer, or a source with the express written authority of the original manufacturer or current design activity, including an authorized aftermarket manufacturer. Unlawful or unauthorized substitutions include used items represented as new, or the false identification of grade, serial number, lot number, date code, or performance characteristics. (c) Vendor shall be an OEM, authorized dealer, authorized distributor, or authorized reseller for the proposed equipment/system, verified by an authorization letter or other documents from the OEM. All software licensing, warranty and service associated with the equipment/system shall be in accordance with the OEM terms and conditions. (End of clause)

View original listing