This fact sheet explains IDMP, a set of ISO standards mandating standardized medicinal product data worldwide, beginning with EMA in 2023. IQVIA’s NLP solution accelerates compliance by extracting 300–2,000 required data entities per product from unstructured documents like SmPCs, licenses, and regulatory dossiers. The approach automates curation, ensures accuracy, and supports evolving frameworks. Case studies show pharma companies using IQVIA NLP to process thousands of multilingual documents with >94% accuracy, saving significant time and resources. The solution ensures agility, scalability, and compliance, helping organizations meet regulatory requirements while reducing manual burden.

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