This solution uses NLP to automate extraction, classification, and analysis of regulatory text, reducing compliance costs. Applications span labeling (cutting comparison time by 95%), regulatory intelligence (automated alerts from FDA/EMA), master data management (IDMP/xEVMPD mapping), and dossier development (OCR + NLP workflows). Case studies show top pharma firms saved FTE resources, improved risk management insights, and enhanced submission quality with discrepancy detection. By combining NLP with generative AI, the platform accelerates regulatory processes, improves data accuracy, and reduces manual workload.

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