This case study highlights how Gilead Sciences uses Spotfire to support regulatory compliance, drug safety, and enterprise operations in a highly regulated pharmaceutical environment. Gilead deployed interactive dashboards across clinical trials, safety monitoring, submissions, and operations teams to enable faster exploratory analysis and trend detection. Spotfire reduced dashboard maintenance, accelerated data refreshes by up to 80%, and consolidated reporting views by 50x. Teams gained early visibility into potential safety issues, improved confidence in regulatory submissions, and saved significant time daily. The platform also enabled internal analytics on analytics, helping leadership track productivity, manage compliance, and prepare for future AI-driven initiatives.

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