IT Capability Statement

Health and Human Services
(DECC) Development Effort Consolidation Contract  (Sub Contract):

DECC: Development Effort Consolidation Contract (DECC) project was to develop an Enterprise Service Oriented Architecture (SOA) that will support mission goals and Provide rapid service delivery. The contract also focused on four major application groups

The project also included Legacy system maintenance / migration and Inquiry Support Function. Design and development for the implementation using Oracle SOA/ADF/Webcenter 11g.Leading ADF Development team for Hospital reporting (HR) team. Migrating Legacy application screen to Oracle
ADF/web center Portal screens. Understanding complex business rules associated with legacy system and migrating to Oracle SOA 11g environment. Developing dynamic database driven questionnaire screens using Oracle ADF for Web based Measures application.

FDA
FDA FURLS (Sub Contract):

Our partners were involved in the FDA project called FDA Unified Registration Listing Systems (FURLS) consisting of different modules like Online Account Administration (OAA), Food Facility Registration Modules (FFRM), Device Registration and Listing Module (DRLM), Drug Facility Registration Module (DFRM) and Alert system.
Our team Used dcmctl utility commands to create remove and configure and manage OC4J components in FDA test, development  and production environment. Created    modified, maintained, and enhanced the Ant scripts for the FURLS module for the migration of current of the art system to ICT21 migration project to make them fully automated, and enhanced the performance.

FDA (Sub Contract)
Structure Function Claims Notification (SFCN) and New Dietary Ingredient (NDI) Worked on eliciting requirements for two applications for the Food and Drug Association (FDA) - Structure Function Claims Notification (SFCN) and New Dietary Ingredient Notification (NDI/NDIN), which would allow manufacturers to submit structure or function claims on their dietary supplements electronically, and also allow the manufacturers to provide FDA with information on new dietary ingredients used in
their dietary supplements. The effort was to bring a paper application process into an electronic form. This application was built using existing codes and use-cases from other similar FDA applications.