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  Home > Consulting, Systems, and Solutions > Pharmaceutical Adverse Events "Reporting and Evaluation" System Printer FriendlyPrinter Friendly  
 
 

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  Pharmaceutical Adverse Events "Reporting and Evaluation" System
Booz Allen Hamilton builds globally deployable pharmaceutical adverse events reporting and evaluation systems as well as drug safety and surveillance services.
Booz Allen delivers custom-built systems for pharmaceutical manufacturers to proactively evaluate the safety profile of their pharmaceutical products worldwide. These adverse events reporting and evaluation systems are Web-based and globally deployable providing a single worldwide adverse events reporting and evaluation tool.

Our Approach

Booz Allen has developed an adverse events toolkit that provides core functionality as the basis to build customized solutions, configured to your specifications. The core system:

  • Integrates workflow management;
  • Provides intelligent regulatory rules;
  • Incorporates distribution rules;
  • Grants authorized users access to a centralized repository of adverse events information from their desktops using standard Web intranet tools.
Booz Allen uses proven system development procedures and techniques to craft technology solutions. Our approach comprises the following steps:
  • Develop system concept of operations and project scope;
  • Define system requirements through user-focused, facilitated workshops;
  • Prepare system design specifications through facilitated Joint Application Design (JAD) sessions;
  • Develop and test production software using Booz Allen's spiral development methodology;
  • Provide user training after production release.

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