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Acodis empowers pharmaceutical and life science organizations to transform document-heavy processes into compliant, data-driven operations. With our Document Intelligence platform, Quality, Regulatory, and CMC teams extract, structure, and validate data automatically from batch records, CoAs, CTDs, and more. Designed for regulated industries, Acodis ensures full traceability, audit readiness, and GMP compliance while reducing manual workload. From R&D, to Quality Assurance and Regulatory Affairs, Acodis helps organizations unlock the full potential of their unstructured data — driving faster release cycles, higher data integrity, and smarter decisions across the product lifecycle. No complex setup. No coding. Just intelligent automation that scales with your document needs.