Healthcare Industry

AI Agents for Healthcare
ERP

HIPAA-compliant AI agents for medical device manufacturing, pharmaceutical distribution, FDA validation, and healthcare supply chain management on Infor ERP.

HIPAA Compliant
FDA 21 CFR Part 11
DSCSA Ready
GxP Validated

Healthcare ERP Challenges

Healthcare and life sciences operate under regulatory frameworks where non-compliance means patient safety risks, FDA warning letters, and criminal liability.

HIPAA Compliance

The Health Insurance Portability and Accountability Act requires encryption of PHI at rest and in transit, access audit logging, breach notification protocols, and Business Associate Agreements for all ERP vendors.

$1.5M average breach penalty

FDA 21 CFR Part 11

Medical device manufacturers must maintain electronic records with audit trails, electronic signatures, closed systems, and validated computer systems per FDA regulations.

Complete e-signature validation

Supply Chain Integrity

The Drug Supply Chain Security Act (DSCSA) and UDI requirements demand end-to-end product serialization, lot traceability, and counterpart detection across distribution networks.

Full serialization by mandate

Quality System Regulations

FDA 21 CFR 820 QSR requires design controls, CAPA management, DHR documentation, and validated production processes for all medical device manufacturers.

Zero tolerance for deviations

AI Agents for Healthcare ERP

Agents built for the regulatory intensity of healthcare -- HIPAA, FDA, DSCSA, and GxP compliance automated.

Healthcare Compliance Audit Simulator

Watch AI agents audit your ERP against HIPAA, FDA, and DSCSA requirements. Real-time gap identification with prioritized remediation.

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Compliance Score
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Compliant
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Gaps Found
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Critical Issues
PHI encrypted at rest (AES-256)45 CFR 164.312(a)(2)(iv)

HIPAA Privacy

Access audit logging enabled45 CFR 164.312(b)

HIPAA Security

Electronic signatures validated21 CFR 11.50

FDA 21 CFR Part 11

Audit trail tamper-proof21 CFR 11.10(e)

FDA 21 CFR Part 11

CAPA process documented21 CFR 820.90

FDA 21 CFR 820

Design controls implemented21 CFR 820.30

FDA 21 CFR 820

Product serialization activeDSCSA Section 582

DSCSA

GUDID submissions current21 CFR 801.20

UDI

Breach notification process tested45 CFR 164.404

HIPAA Breach

Computer system validated (IQ/OQ/PQ)21 CFR Part 11

CSV

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