DIA 2025 Global Annual Meeting

Component Type: Session

Discover how AI-powered regulatory document automation is transforming medical writing across various regulatory medical document types for global pharmaceutical companies. This session presents real-world use cases and a demo of an enterprise authoring platform that integrates seamlessly with Veeva Vault. Experience end-to-end automation—from AI-driven drafting and seamless workflow integration to automated updates, cross-functional reviews, and finalization. Key features include a document template engine with expert-curated templates, automated quality control (QC) for factual accuracy and compliance, and real-time data synchronization. Learn how this solution accelerates timelines, ensures audit readiness, and enhances data integrity through AI integration, while streamlining review cycles and propagating changes across documents.

Speaker

Speaker
Sharon Chen