Enhance Your GxP Compliance with AI-Powered Insights
Verixa Copilot seamlessly integrates with your existing QMS, providing real-time answers, actionable insights, and trusted compliance decisions tailored for the life sciences industry.
Get Demo
Compliance Intelligence Architecture
Verixa Copilot’s AI framework is engineered for compliance-first performance. It integrates regulatory databases (FDA, EMA, ICH), organizational SOPs, clinical records, and operational workflows to provide intelligent, traceable outputs—validated by logic chains and ready for audit.
Works with your QMS, not against it
Enables intelligent deviation handling and RCA automation
Ensures compliance actions are explainable, trackable, and risk-prioritized
Ask any GxP-related question—get an instant, traceable, and regulation-backed answer.
How It Helps:
Reduces hours of manual document lookup
Improves confidence in QA decision-making
Aligns responses with your SOPs and current global regulations
Deviation & Risk Triage
Automatically detect, classify, and escalate deviations based on risk priority. Verixa triages issues in real-time using FMEA logic and contextual metadata.
Stops guesswork in deviation handling
Escalates only what matters
Improves time to resolution by 60–80%
RCA + CAPA Engine
Verixa facilitates intelligent root cause investigations with built-in logic like 5 Whys, Fishbone, and Human Error classification. CAPAs are risk-ranked and matched to recurrence likelihood.
How It Helps:
Reduces repetitive CAPAs and vague RCA narratives
Speeds up QA closure cycles
Ensures traceability for inspections
Live Risk Signals & Audit Readiness
Surface compliance blind spots before they become findings. Verixa scores patterns across deviations, CAPAs, and complaints—surfacing systemic risks early.
Detects multi-site trends in real-time
Sends alerts before audits uncover issues
Provides audit-ready logic for every action