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PerkinElmer
  • 產品
  • 信息學

臨床發展

我們的信息學臨床解決方案通過臨床開發所有階段中實時訪問臨床數據精簡了臨床試驗,允許用戶在數據采集后能立即和數據互動。

臨床試驗通過以下增強:

  • 規定隨訪用方案關鍵方面的探索。
  • 通過識別退出和方案違反事件來確保方案依從性
  • 提供所有數據的早期和頻繁視圖,促進快速數據清理并確保數據質量
  • 利用自服務探索分析減少靜態報告和列表的流失及返工
  • 允許對多個試驗/治療領域重復使用工作流程,節省開發和驗證工作中的時間和金錢。

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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Pharmacovigilance

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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