• 产品
  • 信息学




  • 规定随访用方案关键方面の探索,。⮰
  • 通过识别退出和方案违反事件来确保方案依从性
  • 提供所有数据の早期和频繁视图,。促进快速数据清理并确保数据质量
  • 利用自服务探索分析减少静态报告和列表の流失及返工
  • 允许对多个试验/治疗领域重复使用工作流程,。节地方开发和验证工作中の时间和金钱,。⮰

Medical Review

⮱Missing safety signals is the greatest concern for everyone in clinical development, especially medical monitors who are directly responsible for the well-being of trial subjects. With patient safety as the primary directive and concern for the entire clinical team, processes and technologies that can mitigate safety issues during medical review, in stream, all the time, are the gold standard.

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Risk-Based Monitoring

⮱Our Risk-Based Monitoring Solution is the most effective way to leverage data-driven insights to optimize site performance while improving patient safety. With the changing regulatory landscape, you must assess risk holistically, looking beyond just KRIs, by having the technology in place to ensure full data visibility and capabilities to identify and act on root cause for known risks.

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⮱Built on the best-in-class scientific analytics and data discovery platform, TIBCO Spotfire®, our innovative solution for pharmacovigilance, enables teams to strategically transform their medical review, safety review, and compliance monitoring processes; gain new insights leading to faster identification of safety risks early in development, and reduce the time and costs of preparing for safety team reviews.

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Inside Informatics

21 三月, 2019 | Rob Rittberg
I know what you’re asking, “Is this a marketing turn-of-phrase or an attainable outcome?” A Medical Monitor’s top priority is to protect clinical trial subjects by monitoring safety signals in the data. To that end, what are your medical monitor’s processes and what technology are they using to ensu ...

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