One AI-native suite. Five validated platforms.
Pharmacovigilance, clinical data capture, quality, medical info, and trial budgeting — built to interoperate, validated to ship.
One AI-native suite. Five validated platforms.
Pharmacovigilance, clinical data capture, quality, medical info, and trial budgeting — built to interoperate, validated to ship.
PV.app
All-in-one safety platform
AI-driven pharmacovigilance with automated MedDRA coding, ICSR/PSUR/DSUR generation, and direct gateway submissions to FDA, EMA, MHRA.
eQMS
Stay compliant
AI-powered quality management: document control, CAPA, eLMS, risk matrix, and external signing — deployed in days, not quarters.
EDC + ePRO
Convenient eCRF collection
Unified electronic data capture and patient-reported outcomes with real-time validation, MedDRA/WHODrug coding, and PV integration.
MICC
Medical Information Call Center
Omnichannel medical information with AI copilot, speech-to-text, automatic adverse event capture, and direct PV handoff.
Budgets
Clinical trial budgeting & control
Validated, 21 CFR Part 11–compliant clinical trial budgeting, forecasting, and real-time cost control — wired to EDC, CTMS, and PV.
AI Governance Hub
Explainable AI for medical coding & adverse event classification
The control plane for every AI decision in your safety and clinical workflow — explainable, validated, audit-ready.
Regulatory-grade by design.
Ready to consolidate your eClinical stack?
Talk to us about a 30-minute scoping call. No deck. Just product and your real workflow.