An emerging trend for many life sciences companies is the use of globally dispersed teams to run clinical studies, collect patient data and perform biostatistical and PK/PD analysis. One challenge resulting from this network of multiple partners and outsourcing relationships is the management and oversight of complex PK/PD studies that lack standardization. Regardless of company size, key questions faced by drug development organizations are:

• How to support optimized workflows for PK/PD analysis, modeling and reporting?
• How to efficiently provide high-quality, regulatory compliant storage for PK/PD data?
• How to speed data transfer and information exchange between and among global drug development partners?

This white paper introduces a solution that acts as the central hub to tie global team members together and offer a real time portal into data and reports that can be used to reduce timelines to regulatory submission, enhance data management for multi-study analysis, and support valuable clinical study data in a 'transaction-ready' state for due-diligence and out-licensing.

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