Quality Managment System

Qulaity Managment System

A Quality Management System (QMS) is defined as a formalized system that documents processes, procedures, and responsibilities for achieving quality policies and objectives. A QMS helps coordinate and direct an organization’s activities to meet customer and regulatory requirements and improve its effectiveness and efficiency on a continuous basis.


CAPA Management and Tracking Software is designed to fully integrate with other critical quality systems such as but not limited to Audits.

Market Complaints

Market Complaints Management Software automates the handling of complaints from initial complaint, acknowledgment,

Deviation Management

Deviation Management Software automates the manual process of handling planned.


OOS Management System automates the process of handling Out-of-Specifications.

Change Control

Change Control Module is designed to maintain smooth communication and coordination in order to manage every significant step of Change.

Audit Management

Audit Management and Scheduling Software enable the organizations to manage audit schedules, internal audits.

Vendor Qualification

By being a web-based platform the proposal of new vendors for qualification is easy.


Lab Incident Reporting module is used to automate the manual paper-based process.


Our eQMS Software improves the response times for your both internal and external audits, product releases and required changes.
Capable to provide metrics reporting and analytical trending that gives real life informational reports with an eye-catching visual representation to take a quick decision making.
It can create customized reports, workflow processes that fit the needs of your organization or business processes.

Features of Quality Managment System

eQMS software is a user-friendly system helps to simplify, streamline any tedious tasks and manage your quality control processes. This quality systems software has the ability to automate the tasks, cross-functional team’s collaboration, including routing all documents with proper follow-ups, and escalates necessary triggers to users for task completion, approvals or rejection cycles. This quality management system in pharma will help to reduce risks associated with manual processes, provides better internal communication between teams, reduce costs incurred by reworks, and increase the product quality.