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

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

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

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

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

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

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

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

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

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