For pharmaceutical manufacturers, Adlib is the only AI-enabled document workflow automation platform that transforms complex, unstructured regulatory and clinical documentation into precise, structured, and compliant data pipelines. Whether it's digitizing handwritten batch records, assembling FDA-ready submissions, or validating labeling and QMS documents, Adlib automates what others leave manual—accelerating drug development timelines, ensuring regulatory readiness, and reducing compliance risk.

Adlib acts as the invisible middleware engine that integrates seamlessly with systems like Veeva Vault, MasterControl, TrackWise, and other life sciences QMS and MES platforms, bridging gaps between unstructured documents and structured, audit-ready data that powers downstream workflows.

Trusted by 7 of the top 10 global life sciences organizations, including Pfizer, BMS, J&J, and AbbVie, Adlib is the foundation behind mission-critical document workflows that power drug development, regulatory compliance, and manufacturing excellence.