White Paper: Electronic Drug Accountability Systems

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The increase in federal audits and the growing federal regulations has made drug accountability management a major challenge. A failed federal audit leads to costly trial delays, and possibly non-approval or criminal liability. Electronic drug accountability managed through an IRT system can ensure compliance, reduce inefficiencies, preserve data integrity and increase patient safety.  

This white paper examines how electronic drug accountability managed through an IRT system:



  • Improves protocol compliance

  • Reduces clinical trial inefficiencies

  • Preserves study data integrity

  • Increases patient safety

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