Software Technology for QFT-GIT ELISA Reader

Award Information
Agency:
Department of Defense
Branch
Office of the Secretary of Defense
Amount:
$99,901.00
Award Year:
2007
Program:
SBIR
Phase:
Phase I
Contract:
FA8650-07-M-6720
Award Id:
83003
Agency Tracking Number:
O063-H06-3142
Solicitation Year:
n/a
Solicitation Topic Code:
n/a
Solicitation Number:
n/a
Small Business Information
6525 Belcrest RD, Suite 500, Hyattsville, MD, 20782
Hubzone Owned:
N
Minority Owned:
N
Woman Owned:
N
Duns:
788153166
Principal Investigator:
Raymond Peterson
Chief Science Officer
(301) 683-2118
rpeterson@celadonlabs.com
Business Contact:
Lawrence Kessner
Chief Executive Officer
(301) 683-2117
lkessner@celadonlabs.com
Research Institute:
n/a
Abstract
Tuberculosis is a growing threat to military personnel. The accepted method of preventing tuberculosis disease in military personnel is to screen for latent infection using the tuberculin skin test. In order to overcome the high false-positive and false-negative rates of the skin test, the Air Force is conducting a clinical trial of the Cellestis QFT-GIT test kit. The clinical trial presents the opportunity for a software system that manages and interprets QFT-GIT test data. The deliverable of this Phase 1 SBIR proposal is software that transforms optical density readings from the Triturus ELISA reader into QFT-GIT clinical results. It will communicate electronically with the Triturus using the ASTM standard and it will communicate electronically with CHCS using the HL7 standard. Delivery of this system will establish feasibility of the entire project. Additionally during Phase 1 the proposer will perform a comprehensive requirements analysis for Phase 2. Phase 2 deliverables will include DITSCAP accreditation and software validation as well all other deliverables identified in the requirements analysis proposed for Phase 1. Phase 2 deliverables may include a data management system, software for manual editing of instrument sample layout, configuration of the Triturus software, and analysis of the clinical trial data.

* information listed above is at the time of submission.

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