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Look at paperwork and regulations

Nothing evolves within a vacuum. While today we can transmit reports, research, and more at the click of…

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Journey, Insights, and Learnings from Sanofi’s Implementation In a recent discussion…

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What will the next generation of reporting and analytics in pharmacovigilance be? Will it move the needle on business innovation…

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Concepts once thought to be theoretical are now a reality — from smartphones to space flights. In comparison, the…

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5 Reasons to Move to Automated Safety Document Distribution

The very basis of pharmacovigilance is to detect, collect, monitor, and assess reports on adverse events from drug…

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The management of data within organizations has far-reaching effects, as interconnected data provides valuable insights that can yield positive…

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Most regulatory information management (RIM) systems were designed to capture essential regulatory data elements, e.g., drug substance and drug…

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Managing a clinical trial is no small feat. Documents must be tracked, client sites monitored, notes and findings to…

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The Shift to the Cloud Historically, firms relied heavily on on-premises implementations for their enterprise solutions, including safety systems. Reliance…

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The European Union (EU) Clinical Trials Regulation (CTR) harmonizes the processes for assessment and supervision of clinical trials…

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White Paper: The Evolution of Signal Detection and Management   View More