AI in clinical trials, GxP, and adverse-event detection.
21 CFR Part 11 audit trail integrity, GCP-aligned model validation, AI-driven adverse-event signal detection, and clinical-trial outcome explainability for FDA submissions.
5 modules purpose-built for Pharma
Each sub-module addresses a specific obligation in this vertical that the platform's 12 core modules combine with to give you full coverage.
Adverse Events Monitoring
Pharmacovigilance signal detection with hash-chained audit.
Clinical Trials AI
Subject recruitment-bias detection and efficacy prediction governance.
FDA 21 CFR Part 11
Electronic-records and e-signature integrity.
FDA Pre-Cert
De Novo pathway support and real-world performance monitoring.
GCP Compliance
Good Clinical Practice protocol-deviation detection.
Every vertical inherits all 12 core platform modules
Vertical-specific sub-modules sit on top of Pratvi AI's full platform — model inventory, audit trail, bias monitor, drift, security posture, explainability, and more all apply uniformly across every vertical.
See how Pratvi handles Pharma specifically
30-minute walkthrough. No commitment. Bring your specific regulatory exposure and we'll map it to platform capabilities live.
Request access