Xcellerate® Monitoring - Singapore

基于风险的监控需要多于源数据验证（SDV）来识别数据错误。我们的监控方法的基础以质量设计，我们在规划阶段的研究中建立了质量和设计风险。Xcellerate Monitoring包含医学审查，数据审查和统计监控，以便您可以在临床数据上获得更广泛的更灵活的景点。作为Xcellate临床试验优化套件的一部分，它将使您能够主动保护患者安全性，提高数据质量，降低与临床试验相关的成本，时间，复杂性和风险。

您需要一个单一技术平台，请提供当前性能和潜在风险的近实时视图。我们利用一致的流程和实践来帮助任何规模维护网站监测计划的生物制药公司，将资源重定向到最佳位置，并专注于具有质量差异的正确数据。

Identifying your issues before they impact your trial’s performance is a key component of Xcellerate Monitoring. Our risk-based monitoring solution combines full central monitoring, on-site monitoring, Xcellerate Trial Management and Xcellerate Insights so that you stay informed and make important decisions faster. With a holistic view on the latest data trends, you’ll be in full control to mitigate risks across studies and your entire portfolio.

With the combined powers of Xcellerate Monitoring and the Xcellerate Informatics Platform, you’ll be enabled to identify the best-performing sites and deploy your resources to yield the greatest return. Along with the flexibility to scale up or down and adapt your efforts as your site risk profiles evolve, you can create a fit-for-purpose design that reveals savings while delivering higher quality data.

Presented in a collaborative workspace, Xcellerate Monitoring helps you quickly pinpoint risk through intuitive and powerful user interfaces. From major protocol deviations to individual outliers, you will not only recognize the issues but also act on the data to mitigate problems, escalate issues and instantly communicate with Clinical Research Associates (CRAs). Coupled with alert notifications and an embeddable review workflow, you’ll experience a new level of risk-based monitoring efficiencies to reach complete clinical trial optimization.