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Quality Management

eQMS

Quality Processes Under Control. Compliance Evidence Always Ready.

Electronic Quality Management System for deviations, CAPA, change control, complaints, audits, training and controlled quality workflows with complete audit history.

Secure Cloud / Private Cloud / On-Premise Mobile Support Customizable 6-16 weeks depending on processes and validation scope
Trusted by 100+ Manufacturers across India
eQMS
Best For Pharmaceutical, chemical, healthcare, food, engineering and other quality-regulated organizations
Industry Pharmaceutical, Engineering, Healthcare, General Manufacturing
Category Quality Management
Deployment Secure Cloud / Private Cloud / On-Premise
Type Configurable
Modules 5+ Core Modules
Implementation 6-16 weeks depending on processes and validation scope
Overview

About eQMS

<p><strong>eQMS</strong> is a professionally designed business platform that centralizes critical records, workflows, approvals and reports.</p><p>Electronic Quality Management System for deviations, CAPA, change control, complaints, audits, training and controlled quality workflows with complete audit history.</p><p>GRPTechs configures roles, forms, alerts, dashboards and integrations around the approved operating process so teams receive a practical, scalable and controlled solution.</p>
Challenges

Problems We Solve

Common pain points this software eliminates from your operations

Paper-Based Quality Records

Paper forms are difficult to route, search, monitor and retrieve during review or audit.

Delayed CAPA Closure

Actions remain open because ownership, due dates, reminders and escalation are not centrally controlled.

Disconnected Quality Events

Deviations, complaints, changes, risks and CAPAs are maintained separately, weakening investigation visibility.

Weak Version and Approval Control

Uncontrolled templates and email approvals create uncertainty about the current authorized record.

Limited Management Visibility

Quality leaders lack live views of overdue actions, recurring causes and department performance.

Time-Consuming Audit Preparation

Teams spend excessive time compiling event history, approvals and supporting evidence.

Benefits

Key Benefits

What your business gains after going live

Timely Closure

Faster Quality Event Closure

Ownership, due dates and escalation improve follow-up.

Controlled Process

Stronger Compliance Control

Defined workflows and approvals improve process discipline.

Full History

Complete Traceability

Linked events, investigations and actions remain available in one history.

Paperless Quality

Reduced Paperwork

Digital records reduce printing, routing and manual filing.

Trend Visibility

Better Root-Cause Insight

Structured classifications and trends support recurring-issue analysis.

Audit Support

Audit Readiness

Searchable records and evidence simplify audit preparation.

Live Oversight

Management Visibility

Dashboards highlight overdue and high-risk quality actions.

Growth Ready

Scalable Quality System

Add processes, departments and sites using common controls.

Features

Main Features

Everything included in eQMS

  • Deviation & Incident Management
  • CAPA Management
  • Change Control
  • Audit & Complaint Management
  • Quality Analytics & Administration
Modules

Product Modules

Functional modules included or available with this product

Deviation & Incident Management

Capture, assess, investigate and close quality events.

  • Event Registration
  • Initial Assessment
  • Risk Classification
  • Investigation
  • Root Cause Analysis
  • Action Assignment
  • QA Closure

CAPA Management

Control corrective and preventive actions through completion and effectiveness review.

  • CAPA Initiation
  • Source Linking
  • Action Plan
  • Owner and Due Date
  • Progress Evidence
  • Effectiveness Check
  • Final Closure

Change Control

Evaluate and approve controlled changes with impact visibility.

  • Change Request
  • Business Justification
  • Impact Assessment
  • Risk Review
  • Implementation Plan
  • Verification
  • Post-Implementation Closure

Audit & Complaint Management

Manage audits, observations, complaints and responses in structured workflows.

  • Audit Schedule
  • Audit Checklist
  • Observation Recording
  • Response Assignment
  • Complaint Registration
  • Investigation Link
  • Closure Report

Quality Analytics & Administration

Monitor compliance and configure secure quality operations.

  • Quality Dashboard
  • Overdue Actions
  • Trend Analysis
  • Role-Based Access
  • Electronic Approval
  • Audit Trail
  • Exportable Reports
Process

How It Works

End-to-end workflow supported by this software

1
Requirement Discussion

Understand business goals, lead sources, and sales processes.

2
Sales Process Analysis

Review the existing enquiry and lead management workflow.

3
Solution Design

Design workflows, lead stages, and user roles based on business needs.

4
System Configuration

Configure lead pipelines, automation rules, notifications, and permissions.

5
Integration Setup

Integrate email, WhatsApp, telephony, and third-party business applications.

Sectors

Industries Supported

Pharmaceutical Engineering Healthcare General Manufacturing Finance & NBFC Education Retail
Teams

Departments Served

Management HR Finance IT
Connect

Available Integrations

Tally ERP

Synchronize customer invoices and accounting records with Tally. Integration Name

Available
Microsoft Outlook

Sync emails, calendars, and customer communication.

Available
Security

Security & Access Control

  • Role-Based User Access
  • Approval and Activity Audit History
  • Controlled Master and Transaction Changes
  • Secure Authentication and Sessions
  • Correction and Reversal Controls
  • Scheduled Backup and Recovery
Go Live

Implementation Process

01
Quality Process Discovery

Confirm business requirements, stakeholders, scope and expected outcomes.

02
SOP and Workflow Mapping

Map current activities, dependencies, controls and exceptions with process owners.

03
Validation and Scope Plan

Design the agreed solution structure, responsibilities, approvals and reports.

04
Role and Approval Design

Configure organizational structures, masters, roles and operating rules.

05
Master Data Configuration

Prepare, clean and validate the information required for system setup.

06
Quality Form Setup

Configure forms, workflows, alerts, dashboards and document outputs.

07
Data Migration

Migrate approved data and connect agreed external systems or devices.

08
User Acceptance Testing

Test normal, exception, approval, correction and reporting scenarios.

09
Training and Validation

Train role-based users and complete controlled cutover preparation.

10
Go-Live and Stabilization

Launch the solution, monitor adoption and resolve stabilization observations.

Pricing

Plans & Pricing

Transparent pricing. No hidden charges.

Contact for Pricing

Pricing depends on users, modules, locations, and customization requirements.

Get a Quote
FAQ

Frequently Asked Questions

What quality processes can eQMS manage?
It can be configured for deviations, CAPA, change control, complaints, audits, training, risks and related quality workflows.
Does it maintain an audit trail?
Yes. Configured actions, changes, approvals and status history can be recorded for authorized review.
Can CAPAs be linked to other events?
Yes. CAPAs can be linked to deviations, audits, complaints and other approved quality-event sources.
Can it support multiple sites?
Yes. Sites, departments, roles and reporting structures can be configured according to scope.
Can existing records be migrated?
Approved open records and selected masters can be migrated after mapping and validation.
How long does implementation take?
A typical implementation takes 6-16 weeks depending on processes, validation, data and integrations.
Explore

Related Products

Ready to improve your operations with eQMS?

Share your current process, users, locations and integration needs. GRPTechs will prepare a focused demonstration and requirement-based proposal.

Have a Software Idea or Business Challenge?

Let's build a practical solution together. Tell us what manual or paper-based process you want to digitize - we'll show you how.

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Prabhat Colony Road, Mahad
Raigad, Maharashtra - 402301

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