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description: Review of QEdge Software: system overview, features, price and cost information. Get free demos and compare to similar programs.
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title: QEdge | Reviews, Pricing & Demos - SoftwareAdvice GB
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Breadcrumb: [Home](/) > [Quality Management Software](/directory/420/quality-management-software/software) > [QEdge](/software/291404/qedge)

# QEdge

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> QEdge is a Risk-based Enterprise Quality Management Software (eQMS) built for pharmaceutical and life sciences organisations to streamline and automate their quality processes. Designed for both on-premise and cloud-ready environments, QEdge ensures end-to-end control over quality operations while helping businesses maintain regulatory compliance, enhance product quality, and stay audit-ready. With role-based access, complete audit trails, workflow-driven automation, AI-powered features, and seamless integration with LIMS, ERP, MES, HRMS, and TPA systems, QEdge delivers scalable and intelligent quality management. It is fully validated and aligns with major global regulatory standards, including 21 CFR Part 11, EU Annex 11, GAMP 5, ISO 9001:2015, and GDPR.
QEdge Modules:
•	Process Control
Fully configurable Change Control, CAPA, Deviation, Investigation, Market Complaint, OOS, OOT, Risk Assessment, Audit Management
•	Document Control \& SOP Management
Full document lifecycle management: Creation, Approval, Version Control, Storage, Distribution, Obsolescence, Archival
Issuance workflows: Requisition, Approval, Execution, Retrieval
•	Training \& eLearning
AI-enabled Training Lifecycle: Skill Matrix, Gap Analysis, Calendar-based Scheduling, Execution, Evaluation, Certificates
Supports SCORM, Biometric Authentication, Quiz Randomization, SOP Mapping, and External Training Tracking
•	Vendor Qualification
Centralised platform for Vendor Registration, Document Review, Sample Analysis, Trial Batch Evaluation, Audit Management, and Compliance Reporting
•	Product Quality Review (PQR/APQR)
One-click automated generation with multi-source data collection, processing, and customizable scheduling.
> 
> Verdict: Rated **4.4/5** by 12 users. Top-rated for **Likelihood to recommend**.

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## Quick Stats & Ratings

| Metric | Rating | Detail |
| **Overall** | **4.4/5** | 12 Reviews |
| Ease of Use | 4.8/5 | Based on overall reviews |
| Customer Support | 4.8/5 | Based on overall reviews |
| Value for Money | 4.5/5 | Based on overall reviews |
| Features | 4.6/5 | Based on overall reviews |
| Recommendation percentage | 90% | (9/10 Likelihood to recommend) |

## About the vendor

- **Company**: Sarjen Systems
- **Location**: Ahmedabad 380015, India, India
- **Founded**: 1998

## Commercial Context

- **Starting Price**: US$79.00
- **Pricing model**: Per User
- **Pricing Details**: Please contact Sarjen Systems for pricing details.
- **Target Audience**: 11–50, 51–200, 201–500, 501–1,000, 1,001–5,000, 5,001–10,000, 10,000+
- **Deployment & Platforms**: Cloud, SaaS, Web-based, Windows (Desktop), Windows (On-Premise)
- **Supported Languages**: English
- **Available Countries**: Bangladesh, Canada, India, Iran, United Arab Emirates, United Kingdom, United States

## Features

- API
- Access Controls/Permissions
- Activity Dashboard
- Alerts/Notifications
- Approval Process Control
- Audit Management
- Change Management
- Communications Management
- Complaint Management
- Compliance Management
- Corrective and Preventive Actions (CAPA)
- Customisable Reports
- Data Import/Export
- Defect Tracking
- Document Coding & Control
- Document Management
- ISO Standards Management
- Incident Management
- Quality Control
- Real-Time Data

## Integrations (3 total)

- Employee Training Management
- Vendor Management System
- dls | training management

## Support Options

- Email/Help Desk
- FAQs/Forum
- Knowledge Base
- Phone Support
- 24/7 (Live rep)
- Chat

## Category

- [Quality Management Software](https://www.softwareadvice.co.uk/directory/420/quality-management-software/software)

## Alternatives

1. [MasterControl Quality Excellence](https://www.softwareadvice.co.uk/software/142000/mastercontrol) — 4.5/5 (526 reviews)
2. [KAWAK](https://www.softwareadvice.co.uk/software/357377/kawak) — 4.6/5 (320 reviews)
3. [Qualio](https://www.softwareadvice.co.uk/software/152557/qualio) — 4.6/5 (128 reviews)
4. [Isolocity](https://www.softwareadvice.co.uk/software/79422/isolocity) — 4.7/5 (51 reviews)
5. [Checklist Fácil](https://www.softwareadvice.co.uk/software/382163/checklist-facil) — 4.8/5 (105 reviews)

## Reviews

### "Intas Pharmaceutical User reviews" — 5.0/5

> **Verified Reviewer** | *7 April 2020* | Pharmaceuticals | Recommendation rating: 10.0/10
> 
> **Pros**: Interface is very attractive and application is having user friendly functions.
Reporting system is very useful to present the data.
> 
> **Cons**: There no such thing, as the system gives excellent performance.
> 
> QEdge is user friendly application, all useful functions reduce the manual transactions.
Access of required data through ease search function.
High level security of data.

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### "Compliance to international regulatory norms" — 5.0/5

> **Birendra** | *7 April 2020* | Pharmaceuticals | Recommendation rating: 10.0/10
> 
> **Pros**: Easy to use. You can train any person without any difficulties
> 
> **Cons**: Require more feature to integrate with other software like plan-visas etc.
> 
> Excellent in terms of regulatory compliance for example 21 cfr part 11, EU, MHRA, Brazil etc. It gives great comfort to regulatory auditors in terms of compliance.

-----

### "Customize develop software helps us too much for flow wise working , data archieve and maintaining." — 4.0/5

> **Ritesh** | *6 April 2020* | Pharmaceuticals | Recommendation rating: 7.0/10
> 
> **Pros**: Qedge with different sections of QMS and Training.
> 
> **Cons**: Very good and fast working with ease flow.
> 
> Very good and user friendly.

-----

### "I have used Qedge software for change control, deviation, Investigation, CAPA & Training" — 4.0/5

> **MIHIR** | *4 May 2020* | Pharmaceuticals | Recommendation rating: 10.0/10
> 
> **Pros**: Overall product is easy to understand \& good to work with. The software is easily understandable, we can have all features of our requirement \& regulatory requirement respect to 21 CFR \& Annex 11 for EU. There is no major concern and issue with using this product as i am regular user for this product. it is having feature to integrate the same with other business softwares so that we can configure and fetch the data from other software \& take the benefit and avoid rework.
> 
> **Cons**: I appreciate all the features of this product and i am using this software on daily basis for 2-3 hours a day with no major concern. It can also integrate with other software for other business uses and benefits.
> 
> Earlier we have manual process for logging and tracking QMS \&Training which we have eliminate all paper kind of work and use this electronic software with all features. we have saved paper, man power, time and easily/timely get the comments from CFT team.

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### "QEdge QMS" — 4.0/5

> **Rajesh** | *6 April 2020* | Pharmaceuticals | Recommendation rating: 9.0/10
> 
> **Pros**: This software is profile based and not user-based, this will help not stop organization if any employee absence
> 
> **Cons**: Think of changing the profile without logout, standard graphical outputs from the system. Need to think of dashboard with graphical instead of lines like pending, completed, in-process, ongoing, stage-wise. This will help users no need to count the records at their stage
> 
> Overall very good and it's really user friendly and work can be done based on the user

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## Links

- [View on SoftwareAdvice](https://www.softwareadvice.co.uk/software/291404/qedge)

## This page is available in the following languages

| Locale | URL |
| en | <https://www.softwareadvice.com/manufacturing/qedge-profile/> |
| en-AU | <https://www.softwareadvice.com.au/software/291404/qedge> |
| en-GB | <https://www.softwareadvice.co.uk/software/291404/qedge> |
| en-IE | <https://www.softwareadvice.ie/software/291404/qedge> |
| en-NZ | <https://www.softwareadvice.co.nz/software/291404/qedge> |

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