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Enterprise AI governance with multi-tenant security, SSO, and compliance workflows
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Risk Assessment
60-second AI risk classification
AI Registry
Fleet-wide asset lifecycle
Governance
Maturity radar, RACI, Six Pillars
Enforcement
Policy engine, violations
Advanced
Agent Evals (EDD)
Multi-dimension weighted scoring
Guardian Agents
PII, Bias, Hallucination, Cost
MCP API
Agent-to-agent governance
Regulatory Intelligence
AI-powered regulatory KB
Red-Team Testing
Adversarial AI security
Compliance Roadmaps
Gap to action, automatically
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Regulatory greenlighting
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Find and govern rogue AI
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Control agent independence
Continuous audit
Always-on compliance evidence
Decision firewalls
Block harmful outputs at runtime
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Product
Platform Overview
Risk Assessment
AI Registry
Governance
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MCP API
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Healthcare
Healthcare & Life Sciences
Clinical AI, Prior Authorization, and patient safety governance
Clinical Decision Support
Medical Imaging AI
Prior Authorization
Drug Discovery
Patient Triage Chatbots
EHR Analysis
Regulatory landscape
EU AI Act (Annex III)
classifies medical devices and clinical decision-support AI as high-risk systems requiring full conformity assessment
HIPAA
mandates strict patient data protections that extend to all AI systems processing protected health information (PHI)
FDA AI/ML Guidance
establishes evolving framework for AI as Software as a Medical Device (SaMD) with pre-market review pathways
GDPR (Special Category)
health data receives heightened protection - explicit consent or specific legal basis required for AI processing
MDR (EU)
Medical Devices Regulation adds additional layer of compliance for AI-powered diagnostic tools
Key challenges
Clinical AI classified as
high-risk
- safety-critical systems require rigorous testing, validation, and ongoing monitoring before and after deployment
Health data is "special category" under GDPR - heightened protection requirements make AI training and inference significantly more complex
HIPAA compliance for patient-facing AI agents requires end-to-end encryption, access controls, and audit trails for every interaction
FDA evolving guidance on AI as medical device (SaMD) creates regulatory uncertainty - what's compliant today may not be tomorrow
Hallucination risk in clinical AI is literally life-threatening
- a fabricated drug interaction or dosage could cause patient harm
How KoraSafe helps
Risk classification
identifies clinical AI as high-risk immediately, mapping to EU AI Act Annex III and FDA SaMD categories
Hallucination Detector
guardian agent cross-references clinical AI outputs against medical knowledge bases to flag fabrications
Agent Evals (EDD pipeline)
scores clinical AI on accuracy (20%), safety (20%), and auditability (15%) before deployment
Six Pillars checklist
ensures conformity assessment readiness across all governance dimensions
MCP API
allows clinical AI agents to self-check compliance status before making patient recommendations
42% reduction
in documentation time (industry benchmark) --- freeing clinical teams to focus on patient care
All Solutions