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Product

Pharma Compliance AI

Automate regulatory review, quality documentation, and audit readiness.

Built for outcomes, not demos

A conversational GxP compliance agent purpose-built for life sciences. It answers SOP and regulatory questions with version-pinned citations to the exact controlled document, validates SOPs, detects deviations, drafts CAPA documentation, and logs every interaction to an immutable audit trail — reducing risk in the most heavily regulated workflows.

Deployed on FEME's secure, cloud-native platform, it integrates with your existing systems, keeps humans in control of critical decisions, and scales from a single workflow to enterprise-wide operations.

Typical Outcomes

50%Faster audits
90%Deviation detection
24×7Compliance monitoring
Capabilities

Everything you need, out of the box

Regulatory Review
SOP Validation
Quality Documentation
Audit Support
Deviation Detection
Compliance Monitoring
CAPA Tracking
Submission Checks
Where it's used

Industries we serve with this product

Pharmaceutical
Biotech
Medical Devices
Clinical Research

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Talk to our team about deploying autonomous AI agents across your most critical workflows — securely, at global scale.