USDM’s AI practice is built on demonstrated delivery across pharma, biotech, and medical device clients of every size and stage. Every engagement adds to a growing body of repeatable, validated methodology.
Responsible AI Assurance Framework + 150-vendor TPRM managed service — USDM’s flagship AI governance replication model. OSINT-powered intelligence dashboards across the full vendor portfolio.
AI assessment readout, 8-week POC proposal for EnableIQ™ GxP Document ChatBot, and training curriculum for AI citizen development governance.
AI use case scoring methodology, executive briefing deck, and AI governance framework for a newly-formed biopharma with high-growth AI ambitions.
Full 18-slide interactive AI briefing build — deployed as a client-facing sales enablement tool replacing traditional PowerPoint presentation decks.
GxP AI capabilities briefing across pharmacovigilance, medical affairs, and clinical operations — framed for IT and Quality leadership alignment.
EU AI Act compliance preparation programs — classification, Annex IV documentation, and unified FDA + EU AI Act + ISO 42001 compliance frameworks.
USDM’s AI System Lifecycle Framework, TRUST-AI governance architecture, AIGaaS service blueprint, XAI SOP, and Model Governance Framework — proprietary IP deployed across all engagements.
Cloud Assurance managed subscription delivering continuous GxP compliance across Google, Microsoft, Veeva, ServiceNow, Salesforce, Box, and Oracle platforms.
