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This Combined Synopsis/Solicitation opportunity from Department Of Defense was posted on January 26, 2015. The submission period has ended. Browse the details below for market research, or find similar active opportunities.

Clinical Decision Support Tool

Closed
HT0015-15-T-0002Federal

Contract Overview

Solicitation details, issuing organization, response deadlines, documents, and interested companies for this government contract opportunity.

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General Info

NAICS

511210 - Software Publishers

Place of Performance

Contractor's website will be place of performance., VA, USA

Set-Aside

NONE

Documents

7

Amend0001.pdf

PDF

Amendment_0002__HT0015-15-T-0002.pdf

PDF

Attachment_1_Supplemental_Information.pdf

PDF

Enclosure_1_Minimum_Qualifications.xlsx

XLSX

Enclosure_2_Government_Product_Accessibility_Template_for_Computer_Based_Training.doc

DOC

Enclosure_3_Government_Product_Accessibility_Template_for_Web_Applications.doc

DOC

HT0015-15-T-0002-0003.pdf

PDF

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Timeline

3 updates
PhaseClosed
Posted

Combined Synopsis

Notice updated

The notice description changed.

Notice updated

The notice description changed.

Response Deadline

Deadline has passed

Notice updated

Notice details unchanged. Attachments may have changed.

Submission Closed

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Organization & Contact Information

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AgencyDepartment Of Defense → Defense Health Agency
Contacts2 people available
OfficeFALLS CHURCH, VA, 22042, USA
Office AddressFALLS CHURCH, VA, 22042, USA
Contacts

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DEADLINE

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Prototype development for Battlefield Wound Infection Prevention and Treatment (BWI P&T) Barrier Combination
Solicitation # HT9427-26-R-E020
The Defense Health Agency Contracting Activity is seeking proposals for the development of a Battlefield Wound Infection Prevention and Treatment Barrier Combination prototype. This product must integrate a physical wound barrier with antimicrobial and antifungal properties to prevent systemic infections in combat scenarios. The project aims to advance the technology to a Technology Readiness Level of 7 or 8, requiring the development of a working prototype, the execution of human clinical trials, and the successful submission for FDA approval or clearance. The final product must be individual, compact, waterproof, and maintain sterilization, with a preference for packaging that allows one-handed opening in low-light environments. This effort is being conducted under the prototype Other Transaction Authority 10 U.S.C. 4022, meaning it does not follow standard FAR-based procurement. To be eligible, offerors must be nontraditional defense contractors, small businesses, or provide significant cost-sharing. The estimated period of performance is 48 months, divided into three objectives: prototype demonstration, clinical studies and regulatory submissions, and final FDA clearance. Proposals will be evaluated based on technical capability, management capability, and cost, with payments processed electronically via Wide Area Workflow. All clinical research must comply with Good Laboratory, Manufacturing, and Clinical Practices, and be approved by relevant Institutional Review Boards and the USAMRDC Office of Human and Animal Research Oversight.
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POSTED

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DEADLINE

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