From fragmented intake to continuously structured safety operations
Every inbound artifact is automatically classified, validated, routed, and prepared for downstream pharmacovigilance workflows.
Designed as an AI-Native safety system
graph safety continuously understands, validates, and connects workflows across the pharmacovigilance lifecycle.
Multi-channel Ingestion
Email, PDF, XML, APIs, literature, and partner feeds unified into one intake system.
AI-powered extraction
Patient, drug, event, timeline, and clinical context extracted automatically.
MedDRA classification
Context-aware coding with continuously validated terminology alignment.
Cross-source deduplication
Duplicate detection across literature, partner, and spontaneous reporting channels.
Continuos validation
Completeness, consistency, and compliance checks embedded throughout intake.
Intelligent routing
Artifacts classified and routed automatically across downstream safety workflows.
Built for regulatory environments
Aligned with global pharmacovigilance standards with traceability, auditability, and oversight embedded throughout.
AI-native intake with configurable human oversight
Confidence-based routing allows organizations to calibrate operational automation against regulatory and clinical risk tolerance.
Translate only what requires legal-grade review
graph safety automatically classifies translated content before invoking full legal translation workflows for reportable ICSRs.
Connected downstream safety operations
Structured, validated intake outputs flow directly into downstream pharmacovigilance systems through APIs and machine-readable integrations.
Faster implementation timelines
Deploy within existing safety infrastructure
Reduced migration complexity
No system replacement required
Structured downstream interoperability
Standards-compliant case payloads
Lower operational disruption
Existing workflows remain intact
Regulatory confidence at every step
Traceable AI reasoning, configurable oversight, and structured auditability remain embedded throughout intake operations.
Audit traceability
Complete audit trail from source artifact to downstream system
21 CFR Part 11 compliant
Decison Explainability
AI decision reasoning logged and retrievable for inspection
Model version tracked
Model version tracked
GVP Module VI , ICH E2B (R3) , CIOMS , FDA MedWatch ready.
Role-based verification
Compliance alignment
GVP Module VI , ICH E2B (R3) , CIOMS , FDA MedWatch ready.
Continuously validated
Operationalize every safety signal from Day Zero
Enable faster safety decisions, greater regulatory confidence, and more reliable patient safety outcomes across every source.