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65--VITAL SIGNS MONITOR STANDARDIZATION

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W91YTZ13A4546Federal

Contract Overview

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This contract focuses on the standardization of vital signs monitors across Military Treatment Facilities within the Navy Region Mid-Atlantic Command's area of responsibility. The main goal is to enhance the quality of care by selecting clinically preferred products that balance effectiveness with cost efficiency, ensuring value while maintaining high clinical standards. This initiative seeks to reduce the variety of products by limiting the number of Stock Keeping Units (SKUs), thereby streamlining procurement and inventory management. Vendors offering these products must satisfy rigorous technical specifications and demonstrate that their monitors meet or exceed clinical performance benchmarks. The contract aims to establish a uniform set of equipment that supports consistent care delivery across all facilities involved. Through this region-wide, clinically driven program, the contract promotes both cost savings and improved patient outcomes by focusing on a standardized, high-quality medical device solution.

General Info

Standardizing vital signs monitors across Navy Mid-Atlantic facilities for quality, cost, and consistency.

Agency

N/A

NAICS

339113 - Surgical Appliance and Supplies Manufacturing

Place of Performance

Not specified

Set-Aside

NONE

Documents

0

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Timeline

2 updates
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Organization & Contact Information

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AgencyN/A
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Office AddressN/A
ContactsNo contact information available

Full Description

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The primary objective of this effort is to standardize the quality of care across the Military Treatment Facilities (MTFs) in NRMC's Area of Responsibility (AOR) based on the critical balance of clinical efficacy and value. The intent for this initiative is the standardization of a clinically preferred product(s) and source for institutional medicine requirements at the lowest price. It is also intended for this initiative to result in the reduction of Stock Keeping Units (SKUs). As an NRMC -wide clinically driven program, vendors and products must meet specific technical requirements and products must meet or exceed specific clinical performance expectations as primary considerations. For more details and instructions please see attachments.

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