iQMS

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iQMS

iQMS (Intelligent Quality Management System) is an advanced, cloud-based Quality Management and Compliance Platform designed for regulated industries such as pharma, biotech, manufacturing and healthcare. It automates and integrates all core quality processes - including Document Control, Training, CAPA, Change Control, Issue Management and Audits - into a single, unified system.

With workflow automation, electronic signatures and real-time dashboards, iQMS ensures complete visibility, traceability and compliance across your organization. It transforms manual, paper-heavy operations into a smart, digital and audit-ready quality ecosystem.

Our Products

Highlights

Key Features

Document Management

Automated document lifecycle: creation → review → approval → training → archival.

Workflow Management

Validation and version control across all workflows to ensure the consistency and compliance.

Training Management

Auto-triggered workflows for new SOPs, CAPA findings and, new onboardings or audit actions.

Change Control

Automated, role-based routing for review, approval, and implementation.

Issue Management

Centralized issue logs (CAPA) for deviations, complaints & incidents.

Audit Management

Automated CAPA integration audit findings trigger follow-up actions and reviews.
Process

How It Works

Configure

Set up workflows for documents, training, CAPA and audits based on your quality

Automate

iQMS routes tasks, sends notifications and records approvals using e- signatures.

Collaborate

Teams review, approve and act on tasks in real time across departments and sites.

Monitor

Dashboards provide instant visibility into compliance status, bottlenecks and

WHY CHOOSE US

Why IQMS

All-in-One Quality Platform

Unifies document, training, CAPA, audit and change control management.

End-to-End Automation

Eliminates manual errors and reduces cycle times.

Real-Time Visibility

Monitor compliance performance through live dashboards and analytics.

Fully Compliant

Meets FDA, ISO, GxP regulatory standards.

Closed-Loop Quality

Links all processes from issue to resolution for full traceability.

Highly Configurable

Adapt workflows, roles, and forms to your organization’s structure.

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FAQ’s

What industries can use iQMS?

iQMS is ideal for pharmaceutical, biotechnology, medical devices, manufacturing and life sciences organizations that require strict quality and compliance control.

Yes. iQMS is fully compliant with FDA 21 CFR Part 11, ISO, GxP and Annex 11 standards for electronic records, signatures and quality processes.

Absolutely. iQMS can integrate with ERP, LIMS or HRMS systems for seamless data flow and process synchronization.

How does iQMS help during audits?

iQMS maintains audit-ready records including version histories, e-signatures and full traceability ensuring easy inspection and compliance reporting.

Yes. It’s a scalable, multi-site platform with role-based access control and centralized visibility.

You can generate CAPA, training, audit, issue and document compliance reports instantly in PDF or Excel format complete with timestamps and user actions.

Contact US

Ensure Quality and Compliance with iQMS

Automate audits, CAPA, training, and document control — manage all quality processes in one cloud platform.

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