Technical Product Brochure
feme.solutions
Pharma Compliance AI
Automate regulatory review, quality documentation, and audit readiness.
50%
Faster audits
90%
Deviation detection
24×7
Compliance monitoring
Overview
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.
Key capabilities
- Regulatory Review
- SOP Validation
- Quality Documentation
- Audit Support
- Deviation Detection
- Compliance Monitoring
- CAPA Tracking
- Submission Checks
Industries
Enterprise-grade by default
Grounded & cited
RAG with hard data walls — agents cite sources and never invent facts (≥95% faithfulness).
Secure & multi-tenant
RBAC, per-tenant isolation, encryption, and full audit trails. SOC 2-ready.
Human-in-the-loop
Configurable approval gates keep people in control of high-stakes decisions.
Offline-first & private
Runs without third-party API keys when required — sensitive data stays on your infrastructure.
Cloud-native & API-first
Integrates with your CRM, ERP, and ticketing; scales from one workflow to enterprise-wide.
Talk to us
sales@feme.solutions · +919901222551
India · Bengaluru - 560055, KA
Request a demo at feme.solutions/contact