For any organization delivering products and services to customers and patients, Quality is more important than ever, and Technology and Digitalization can be the enablers. QUMAS from Dassault Systèmes is a fully integrated, data-centric, cloud-based Quality Management solution that allows you to automate quality processes, promote data integrity, reduce compliance risks and achieve Quality and Compliance Excellence.
The core of this integrated offering is QUMAS EDMS (Electronic Document Management System) for data-centric Documentation and Content Management and QUMAS EQMS (Enterprise Quality Management System) for Quality Process Management. Both systems are accessible through the user-friendly MyQUMAS interface.
From MyQUMAS you can manage and collaborate in real-time on all regulatory and quality content, create and perform tasks from incident logging through investigation to approval and remediation and access eLearning to browse, view and mark documents as read and understood and to print and search.
QUMAS manages the entire range of quality content and processes supporting SOP updates necessitated by a Deviation or CAPA, all within one unified validated solution. It’s scalability and ability to be deployed in the cloud make it suitable for small to large enterprise implementations.
Designed for regulated industries, QUMAS supports regulatory compliance with US FDA, EMA and PMDA requirements, while reducing validation efforts and inspection/audit times. Additional Quality Intelligence capabilities allow you to search and analyze your Quality data for proactive quality decision making.
QUMAS Customers report
- 80% reduction in approval times
- 40% time improvement for First-to-File / First-to-Market
- 98% cost reduction versus a traditional repository with disconnected systems
QUMAS customer value
Compliance
Data integrity, electronic signatures and an immutable audit trail
Single source of truth
Easy to track, monitor, trend and report on quality from a single data repository
Shorter inspection time
Immediate access to data and documents with interactive dashboards
Deviation tracking
Track performance against SOPs, identify deviations and manage information in a single system
Change control
Managing change orders and conducting impact analysis
Low cost-of-ownership
Cloud-based solution, easy to configure, vendor-managed
Productivity and efficiency
Automated, standardized and streamlined processes
Collaboration
Secure, effective collaboration on documents and content
Overview and control
True end-to-end control and visibility with tailored analytics and dashboards
Shorter time-to-market
Faster approval cycles and fewer rework/recalls
Culture of Quality
A comprehensive, data-centric approach to Quality
To learn about additional BIOVIA capabilities for Total Quality Management watch this video:
MyQUMAS
Access and collaborate with MyQUMAS on all QUMAS regulatory, quality and compliance tasks with one view.
- Manage and collaborate in real-time on all regulatory content throughout the lifecycle.
- Create and perform tasks across CAPAs, Deviations, Audits, Change Controls and Customer Complaints from incident logging through investigation to approval and remediation.
- Access and register for eLearning; browse, view and mark documents as read and understood; print and search.
