Document every AI-assisted clinical decision with tamper-evident audit trails. Automated compliance scoring against HIPAA audit control requirements. Export-ready reports for regulators and internal audits. Plans from $29/month.
Clinical decision support systems, AI-assisted diagnostics, and predictive analytics are transforming patient care. But HIPAA's audit control requirements (§164.312(b)) weren't written with AI in mind. Every time an AI system processes ePHI to generate a clinical recommendation, that interaction must be documented. Most EHR audit logs only capture access — not the AI's reasoning or the clinician's response.
HIPAA's Security Rule mandates audit controls, integrity protections, and documentation retention. Here is how Compliora addresses each requirement.
Implement mechanisms to record and examine access to ePHI.
Every AI-assisted decision is logged with timestamps, user identity, data accessed, and action taken.
Protect ePHI from improper alteration or destruction.
Records are sealed with SHA-256 hashes. Any tampering is detectable and flagged.
Guard against unauthorized access to ePHI during transmission.
All data is encrypted in transit (TLS 1.3) and at rest. No PHI leaves your Compliora workspace.
Maintain policies and documentation for 6 years from creation.
Compliora retains all records with full version history. Export anytime as PDF or JSON.
From diagnostic AI to drug interaction screening, Compliora captures the decision process — not just the outcome.
Document every AI-generated diagnosis suggestion, treatment recommendation, or risk assessment alongside the clinician's actual decision and reasoning.
Example workflow
AI suggests Condition X with 87% confidence. Clinician reviews, considers patient history, documents decision to investigate Condition Y instead.
Track AI-flagged findings in medical imaging and document radiologist review, confirmation, or override with clinical rationale.
Example workflow
AI flags potential anomaly in scan. Radiologist reviews, confirms finding, adds clinical context and follow-up recommendation.
Record AI-powered medication interaction alerts and pharmacist decisions — approvals, overrides, and dose adjustments with justification.
Example workflow
AI flags potential interaction between medications. Pharmacist reviews patient context, documents clinical rationale for proceeding.
Document AI-driven patient risk scores and clinical team decisions about care pathways, resource allocation, and intervention timing.
Example workflow
AI assigns high readmission risk score. Care team reviews, considers social determinants, adjusts care plan and documents reasoning.
Healthcare organizations with EU operations or patients face dual compliance obligations. Compliora analyzes every decision record against both HIPAA and EU AI Act requirements simultaneously. One workflow, two frameworks, complete coverage.
Free tier includes 5 records per month. No credit card required. Upgrade when your clinical team needs to scale.
Yes. HIPAA's audit control requirements (164.312(b)) mandate recording access to and actions taken on electronic protected health information (ePHI). When AI systems process ePHI to generate clinical recommendations, the access, the AI output, and the clinician's response must all be documented. The HHS has increasingly emphasized AI transparency in healthcare settings.
Compliora is designed for documenting AI decision processes, not storing patient records. You record what AI recommended, what the clinician decided, and why — without embedding raw patient data. For workflows that reference patient cases, use de-identified case IDs. All data is encrypted in transit and at rest.
Compliora addresses the AI decision documentation gap that most compliance programs miss. It covers audit controls (164.312(b)), integrity verification (SHA-256 hashing), and documentation retention (164.530(j)). It works alongside your existing EHR, compliance tools, and policies — not as a replacement for them.
EHR audit logs track who accessed what record and when. Compliora tracks the AI decision process: what did the AI recommend, what did the clinician decide, what was the reasoning, and how does the decision align with compliance requirements. This is the documentation layer that sits between the AI tool and the medical record.
Yes. Compliora supports multiple regulatory frameworks simultaneously. A single decision record can be analyzed against both HIPAA and EU AI Act requirements. Healthcare organizations operating in the EU or treating EU patients can maintain compliance with both frameworks from one platform.
Compliora supports EU AI Act, HIPAA, MiFID II, DORA, and 5 additional regulatory frameworks. Each record can be tagged with multiple frameworks and analyzed against all applicable requirements. Cross-framework compliance is built in, not bolted on.