Integrated cloud platform advances speed, efficiency, and accuracy for complex sponsor trial protocols.
With real-time, 24x7 visibility, you can easily collect and manage the increasing volume, variety, and velocity of clinical trial data.
You can get actionable data that allows you to drill down and navigate through the various forms, and perform actions right away.
With a standards-based cloud and integrated workflows, you can accelerate data collection, reduce the timelines, and support regulatory compliance with complete audit trails.
By incorporating genomic data into clinical R&D for patient stratification, you can target drug development and reduce study cost, size, and duration.
You can streamline cleansing and transformation with advanced, standards-based mechanisms that enable operational reuse.