Case Study: Redica Systems achieves reduced compliance risk and major time savings with GoodData

How To Reduce Compliance Risk for Pharmaceutical and Medical Device Companies

Redica Systems is a Quality and Regulatory Intelligence (QRI) platform that ingests and analyzes regulatory and inspection data from agencies like the FDA and EMA to help pharma and medtech companies manage inspection preparation, vendor quality monitoring, and regulatory surveillance. The company faced a major challenge: millions of points of unstructured, siloed data that life sciences firms had been processing manually—slowly and inefficiently—making it hard to surface actionable insights and reduce compliance risk.

To solve this, Redica partnered with GoodData to embed interactive dashboards and visualizations (via GoodData’s React SDK), leverage a semantic layer and logical data model, and run analytics across 50 tailored workspaces—including its Supplier Risk Score™. The result: previously inaccessible data (62k+ documents, 900k+ inspection records) is now structured, interlinked, and visualized for users, saving hundreds of staff hours monthly and driving adoption across more than 200 customers and over 90% of top pharma and medtech companies.

Redica Systems

Arijit Saha

Chief Technology Officer