Non-destructive Viral ID
ID: HR0011SB20254-01Type: Phase II
Overview

Topic

Non-destructive Viral ID

Agency

Agency: DODBranch: DARPA

Program

Type: SBIRPhase: Phase II
Timeline
    Description

    The Department of Defense, through DARPA, is soliciting proposals for the development of a non-destructive viral identification technology under the SBIR program (HR0011SB20254-01). The objective is to create a portable, low size, weight, and power (SWaP) system capable of rapidly identifying viruses in the field without compromising sample viability, addressing the limitations of current methods that often destroy samples. This initiative is critical for enhancing biodefense capabilities, particularly for warfighters deployed in emerging disease hotspots, as it aims to leverage recent technological advances in microfluidics, high-resolution imaging, and metasurfaces. Proposals for Direct to Phase II (DP2) must be submitted by January 8, 2025, with the project expected to span 24 months, including multiple demonstrations and milestones focused on sensitivity, speed, and scalability. Interested parties can find more information and submit proposals through the official solicitation link at https://www.dodsbirsttr.mil/topics-app/.

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    The document outlines a government solicitation for the development of a non-destructive viral identification technology under the HR0011SB20254-01 request. The objective is to create a portable, low power, and lightweight system that can identify viruses in the field without compromising sample viability. Current identification methods often destroy samples, limiting further analysis. The project seeks to leverage advances in technology such as microfluidics, high-resolution imaging, and metasurfaces. Phase I invites Direct to Phase II proposals, requiring candidates to demonstrate the ability to identify various viruses rapidly and provide a pathway toward a scalable portable system. In Phase II (24 months), developers will enhance the system’s accuracy, diversity of viral detection, and sample handling, with multiple demonstrations planned throughout the development process. Successful technology could have significant implications for both defense and commercial industries, facilitating rapid on-site pathogen identification and enhancing biological surveillance capabilities. The document specifies milestone metrics for both phases, emphasizing sensitivity and speed, indicating the Defense Department’s commitment to improving biodefense capabilities.
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