Quality Management System for Diverse Industries
Digitize, Control, and Elevate Quality with Automation and AI
Ensure compliance, reduce risk, and drive continuous improvement with a modern, AI-enabled Electronic Quality Management System.Our Unified eQMS platform centralizes all quality processes—Deviations, CAPA, Change Management, Audits, Complaints, and Risk—into a single, validated system. Built with real-time workflows, full audit trails, and an AI-powered quality agent, it enables both operators and management to make faster, compliant, and data-driven decisions.
What Our Unified eQMS Platform Does
Our Electronic Quality Management System (eQMS) helps regulated organizations manage quality processes across Pharmaceuticals, Life Sciences, Medical Devices, Food Processing, Manufacturing, and Healthcare.
The platform enforces GMP-compliant workflows, automates documentation, and ensures end-to-end traceability across the quality lifecycle.
With an embedded AI-powered Quality Agent, users can instantly query deviations, CAPAs, audit findings, trends, and compliance risks—without manually navigating reports.
Step 1
Document Management System (DMS)
Controlled SOPs, policies, forms, versioning, approvals, and training linkage.
Step 2
Deviations & Non-Conformance (NC)
Structured deviation capture, root cause analysis, and impact assessment.
Step 3
CAPA Management
Risk-based CAPA initiation, effectiveness checks, and closure tracking.
Step 4
Change Management
Controlled changes with impact analysis across products, processes, and documents.
Step 5
Audit Management
Internal, supplier, and regulatory audits with findings, responses, and closures.
Step 6
Training Management
Role-based training assignments linked to SOPs and changes.
Step 7
Risk Management
ICH Q9-aligned risk identification, mitigation, and residual risk tracking.
Step 8
AI-Powered Quality Agent
An AI assistant that answers operator and management questions across the entire QMS in real time.
Key Features of Our eQMS
Quality Process Management
Digitize and standardize all quality workflows with configurable, validated processes
Deviations, CAPA & Change Control
End-to-end traceability between deviations, root causes, CAPAs, and changes—no silos.
Audit-Ready Compliance
Complete audit trails, e-signatures, timestamps, and ALCOA+ compliance by design.
Auditing
Keep comprehensive records of all asset-related activities. From maintenance logs to user actions, our platform ensures compliance with industry regulations and simplifies the audit process.
AI-Powered Quality Agent
Ask questions like:
- “Why are deviations increasing in Line 3?”
- “Which CAPAs are overdue and high-risk?”
- “What changes impacted Product X in the last 6 months?”
The AI delivers instant, explainable answers.
Automation & Workflow Orchestration
Rule-based workflows, escalations, reminders, and approvals—fully automated.
Risk-Based Quality Intelligence
Trend analysis, recurring issue detection, and early warning signals.
Training & SOP Alignment
Ensure only trained users execute approved procedures—always audit-safe.
Inventory & Spare Management
Monitor spare parts and inventory levels in real time to avoid shortages or excess stock. Ensure that your maintenance teams have the necessary resources to respond quickly to any asset-related issue.
Industries We Help
Our Quality Management System is designed to meet the unique demands of diverse industries. Whether you’re ensuring regulatory compliance, managing audits, or driving continuous improvement, our platform empowers you to achieve operational excellence
Pharmaceuticals & Life Sciences
Pharmaceutical organizations operate in highly regulated environments where compliance and traceability are critical. Our Unified eQMS enables you to:
- Manage deviations, CAPA, and change control in a GMP-compliant manner
- Maintain complete audit trails for regulatory inspections
- Ensure SOP, training, and quality process alignment
- Gain real-time visibility into quality trends and risks
- Use the AI-powered quality agent to respond quickly to inspection and management queries
Medical Devices
Medical device manufacturers require strict control over quality and risk throughout the product lifecycle. Our platform helps you:
Manufacturing
Manufacturing organizations need consistent quality execution across plants and operations. Our Unified eQMS allows you to:
Healthcare & Laboratories
Healthcare and laboratory environments require controlled processes and documentation accuracy. Our platform helps you:
How Our eQMS Platform Helps You
Our Unified Asset Management Platform provides a comprehensive solution to streamline asset management, reduce operational costs, and improve efficiency across your business. With real-time automation and an AI-powered assistant, you gain control and visibility into every aspect of asset management.
Inspection Ready, Always
Audit-ready data with zero spreadsheet dependency.
Reduced Compliance Risk
Early detection of trends and systemic quality issues.
Faster Closures
Automation and AI reduce cycle times for deviations and CAPAs.
Management Visibility
Real-time dashboards and AI-driven insights for leadership.
Scalable & Configurable
Multi-site, multi-product, multi-regulation support.
Do You Have Questions on Your Mind?
We know that choosing an quality management platform can come with questions. Here are the most common queries we receive about our Quality Management Platform:
FAQs
What is an Electronic Quality Management System (eQMS)?
How is eQMS different from a basic QMS or CRUD system?
How does the AI-powered Quality Agent help?
Is the platform GMP and 21 CFR Part 11 compliant?
“
Get Started with Unified eQMS
Modernize your quality operations with an intelligent, compliant, and future-ready eQMS.
Move beyond documentation—towards Quality Intelligence.
