QEdge Overview of Reviews & Product Details - 2025
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QEdge
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QEdge is a 21 CFR and EU Annex 11-compliant Enterprise Quality Management System (eQMS) designed for the pharmaceuticals, manufacturing, and life sciences industries. It streamlines quality processes, automates document control, and enhances training management, helping organizations reduce compliance risks and improve efficiency. QEdge offers flexible modules for various workflows like CAPA, deviations, market complaints, vendor qualification, and training management, tailored to meet business-specific needs. It reduces manual paperwork, ensures data reliability, and simplifies regulatory audits with feature-rich, user-friendly interfaces.

Overview

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Streamline Quality Management with QEdge – A Comprehensive eQMS Solution

QEdge, a robust enterprise Quality Management System (eQMS), is designed to automate quality processes and ensure compliance for businesses in pharmaceuticals, life sciences, and manufacturing....

Streamline Quality Management with QEdge – A Comprehensive eQMS Solution

QEdge, a robust enterprise Quality Management System (eQMS), is designed to automate quality processes and ensure compliance for businesses in pharmaceuticals, life sciences, and manufacturing. Developed by Sarjen Systems, QEdge optimizes workflows with features that reduce risks, enhance organizational compliance, and support cost-effective operations.

Why Use QEdge?

In the realm of quality management, QEdge excels with:

  • Process Control Automation: QEdge provides modules for managing Change Control, CAPA, Deviations, Investigations, Out of Specification (OOS), Out of Trend (OOT) issues, and market complaints, ensuring seamless workflows and quick resolutions.
  • Document Control: Efficiently organize and manage Standard Operating Procedures (SOPs), protocols, procedures, and workflows, with robust tracking and version control.
  • Training Management: Comprehensive tools for eLearning, records management, and scheduling enable effective team training and competency development.
  • Regulatory Compliance: Its compliance with global standards such as 21 CFR Part 11 and EU Annex 11 ensures adherence to international regulatory requirements with audit trails and data integrity.
  • User Access and Security: A role-based user management system provides strong data security and controlled access tailored to organizational structures.
  • Customizability: Adaptable features and modules allow businesses to customize workflows according to unique processes without compromising compliance or performance.

Who is QEdge For?

QEdge is ideal for organizations that prioritize quality, compliance, and operational efficiency:

  • Pharmaceutical and Life Sciences Companies: Streamline quality workflows, manage regulatory compliance, and integrate training for industry-specific needs.
  • Manufacturers: Automate quality processes and reduce manual dependency, ensuring improved product compliance and reduced operational risks.
  • Quality Assurance Teams: Use advanced reporting and audit-ready functionality to meet stringent industry standards.

In summary, QEdge is a versatile eQMS platform offering an end-to-end solution for quality, training, and document management. Its customization capabilities, regulatory compliance, and user-friendly design empower businesses to efficiently tackle quality challenges while fostering a culture of continuous improvement.

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73% Subscribed Score
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$6.58/Month
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To cancel a QEdge product:

  • Click the “cancel” button if you do not agree to the terms.
  • Sign out and avoid further use of the company’s products.
  • Note that cancellation is based on acceptance of the terms and conditions.
FAQ

Most frequent question about QEdge

What is QEdge and what industry is it designed for?

QEdge is an enterprise-wide Quality Management System (QMS) specifically designed for pharmaceutical manufacturing.

What key features does QEdge offer?

QEdge offers features such as Process Control, Document Control & Issuance, Training Management System, Vendor Qualification Management, Product Quality Review (PQR), Audit Management System, Trend Analysis, New Product Introduction, Artwork Management System, and User Access Management.

What regulatory compliance does QEdge adhere to?

QEdge complies with regulations such as GxP, FDA 21 CFR Part 11 and Part 820, EudraLex Annex 11, GAMP 5, ISO 9001:2015, and GDPR.

How does QEdge enhance user experience and efficiency?

QEdge enhances user experience through its user-friendly interface, automated workflows, process versioning, and powerful reporting systems, which reduce manual transactions and paperwork.

Can QEdge be customized to meet specific company requirements?

Yes, QEdge can be customized to meet specific company requirements, allowing for tailored process flows and integration with other business software.

Alternatives

Try these alternatives of QEdge

Teamcenter is a powerful product lifecycle management (PLM) solution designed to streamline processes and enhance collaboration across teams. It provides robust tools for managing product data, engineering workflows, and multi-domain bill of materials (BOM). With deployment options including on-premises, cloud, and SaaS, Teamcenter facilitates innovation and improves product development efficiency. Its user-friendly interface enables organizations to optimize product lifecycles and ensure data accuracy.