Sample Collection and Processing Methods to Support Battlefield Wound Infection Diagnostics (Direct to Phase II)
ID: DHA244-D001Type: BOTH
Overview

Topic

Sample Collection and Processing Methods to Support Battlefield Wound Infection Diagnostics (Direct to Phase II)

Agency

Department of DefenseN/A

Program

Type: SBIRPhase: BOTHYear: 2024

Topic Link

https://www.sbir.gov/node/2601961

Additional Information

https://www.defensesbirsttr.mil/SBIR-STTR/Opportunities/
Timeline
    Description

    The Department of Defense (DOD) is seeking proposals for a Small Business Innovation Research (SBIR) program focused on the topic of "Sample Collection and Processing Methods to Support Battlefield Wound Infection Diagnostics (Direct to Phase II)". The Defense Health Agency is the specific branch of the DOD overseeing this topic. The objective is to develop a simple-to-use sample collection and processing method that can accurately detect specific fungal and bacterial species commonly associated with complex battlefield wound infections. The technology should be capable of preparing an adequate specimen for identification and detection in far-forward deployed environments. The current diagnostic capabilities for battlefield wound infections are limited and time-consuming, leading to delays in treatment and medical intervention decisions. The proposed technology should provide rapid diagnostics with a sample collection-to-result time of less than 2 hours, improving patient outcomes and reducing morbidity and mortality. The technology should be compatible with wet/dry environments, require minimum logistical support, and be stable in long-term storage. It should also be easy to use with little training and provide unambiguous primary output. The technology must include a plan for FDA clearance and should align with CLIA-waived complexity standards. The SBIR program consists of three phases: Phase I focuses on demonstrating scientific and technical feasibility, Phase II involves refining the technology and integrating it with a rapid diagnostic platform, and Phase III aims to secure FDA approval and commercialize the technology for both civilian and military settings. The government may propose further harmonization of the technology with other relevant products to meet additional DoD requirements. The solicitation is open until March 31, 2025. More information can be found on the grants.gov website or the DOD SBIR/STTR Opportunities page.

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