• Regulatory complexity and compliance risk across HIPAA, FDA, and CMS rules
• Fragmented, unstructured knowledge scattered across EHRs, PDFs, and clinical guidelines
• Rapidly evolving evidence and protocols that are difficult to keep current and consistent
✓ 60% faster content production cycle time from draft to publish
✓ 40% reduction in authoring and editing costs vs. manual processes
✓ 25% fewer compliance revisions per release through automated QA