Edge Out Your Quality Management Hassles

With our Enterprise Quality Management System

Explore the Power of Quality Management

For Pharmaceutical & Life Science Industries

Manage Core Functions of GRC

With a Single Integrated Package

Explore the Power of Electronic Quality Management 

    QEdge eQMS

    This Industry ready solution for Pharma & Life Science is a GxP compliant enterprise wide quality management system that configures all the quality events on a single platform. It provides high level of flexibility of configuration according to individual business scenario. With an experience of more than 25 years of workflows in the industry, and the mix of technology expertise, Sarjen has developed the right systems to edge out your quality management hassles.


    Celebrating 25 Years of Trusted Partnerships

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    Users

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    Countries

    User Driven Dashboards & Custom Reports

    Seamless Integration with other ERP/LIMS/MES

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    Regulatory Audits Passed

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    Quality Process Configured

    QEdge Quality Management System Suite

    01

    Quality Events’ Management

    Catalyze quality with effectiveness

    QEdge eQMS solution helps organizations to manage their QMS process with poise. It brings all the quality documents like market complaints, investigation, CAPA, deviation, risk assessment, OOS, OOT change control and many more on a single platform.

    02

    Document Management

    Manage complete lifecycle of document

    QEdge DMS ensures that documents such as manuals, SOPs, work instructions, specifications, BMRs are managed and retrieved efficiently. It also helps tracking document distribution, retrieval and maintaining records of distributed copy.

    03

    Training Management

    Share and manage training data across the company
    QEdge eLearning management software (lms) solution encapsulates eLearnings, trainings record management and training scheduling, all on a single platform.
    04

    Product Quality Review (PQR)

    Auto Generate PQR Documents

    QEdge PQR offers automation and digitization ensuring data integrity. It is compliant with all major standards including 21 CFR PART 11 and EU Annex 11 Standards.

    05

    Vendor Qualification

    Simplify Vendor Data Management

    QEdge VQM assures that materials procured are produced, packaged, and shipped under a controlled process that results in consistent quality conformance and meets regulatory expectations.

    QEdge Customer Speaks

    “Compliance to international regulatory norms”
    Birendra S.
    SVP

    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.

    Easy to use. You can train any person without any difficulties

    We customized QEdge as per our company requirement. So that process flow did work exactly same as per our defined procedure.

    How QEdge helps your peers in Pharmaceutical & Life Science Industries

    Digitalization of Corporate Guidelines

    The Corporate Quality Assurance department centrally ensures QUALITY across all the manufacturing sites of an organization.

    View Case Study

    Digitalization of 6M Investigation

    Investigations of production and industrial operations problems are a very integral part of any pharmaceutical or life science industry.

    View Case Study