Industry Briefing · Free PDF
Autonomous agents on document-heavy, regulated clinical and pharma work.
How to put agents on regulated clinical and pharma processes by separating two things cleanly: agents collect, verify, reconcile and keep the record, while the clinical and regulatory decision stays with your people.
What's inside
- Five document-drowned processes: clinical documentation, prior authorization, pharmacovigilance intake, regulatory submissions, and quality documentation.
- The four governance disciplines for probabilistic agents, mapped onto dossier-heavy clinical and pharma flows.
- A compliance map linking EU AI Act, GDPR special-category health data, MDR, IVDR, EU GMP Annex 11 and ALCOA+ to a control.
- A pharmacovigilance-intake blueprint end to end, and a 30/60/90 Foundation with an explicit go/no-go gate.
Industry briefing · PDF · Healthcare & Pharma
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