The smarter alternative to QT9 for life sciences teams
Matrix Quality delivers a Salesforce-native eQMS with modern UX, rich analytics, manufacturing management, advanced regulatory & TMF capabilities, and rapid implementation — so you can focus on quality, not your software.
This comparison is based on publicly available information and internal analysis as of March 2026. Features and capabilities may change over time. For the most accurate and up-to-date information, you can refer to the official website of QT9 QMS
Common frustrations with QT9 QMS
Teams evaluating QT9 for growing life sciences operations consistently report the same limitations.
What changes when you switch to Matrix Quality
Maintain quality and traceability with a simple workflow
All-in-one QMS solution managing compliance, quality, and operations
Complex regulatory requirements
From FDA and EMA to ISO and GxP standards, maintaining continuous compliance is resource-intensive and demands consistent documentation, traceability, and audit evidence across all quality processes.
Compliance
Pre-configured workflows and templates aligned with FDA 21 CFR Part 11, ISO 13485, and GxP standards — so your team spends less time building compliance infrastructure and more time on quality outcomes.
Data silos and inefficient processes
Fragmented documentation across quality, manufacturing, and regulatory teams makes it difficult to ensure data integrity, traceability, and a single source of truth.
Unified Platform
Centralised control of documents, CAPAs, change management, training, audits, manufacturing, TMF, and regulatory submissions — eliminating data silos and reducing the number of systems your team must manage.
Audit readiness
Preparing for inspections and demonstrating end-to-end control over quality events can stall innovation and slow time-to-market when records are scattered across disconnected systems.
Real-Time Visibility
Advanced analytics and dashboards — powered by the Salesforce platform — give quality leaders actionable insights across all quality processes without needing a separate BI tool.
Scalability and global operations
As organisations grow, managing quality consistently across multiple sites, partners, and product lines with a platform that lacks deep Salesforce ecosystem integration becomes increasingly limiting.
Scalable & Secure
Cloud-based, Salesforce-native architecture designed to grow with your organisation while maintaining strict data security, traceability, and enterprise-grade performance at scale.
Limited analytics without additional tools
Quality leaders need real-time insights to drive continuous improvement, but relying on separate BI tools for advanced analytics creates additional cost, maintenance, and data consistency challenges.
Reduced validation effort
Significantly reduced through pre-configured, validation-ready workflows, clear traceability, and a risk-based approach aligned with GxP expectations.
No AI to accelerate quality processes
Manual workflows for document creation, CAPA investigation, and risk analysis are slow and error-prone. Without AI assistance, quality teams spend more time on administrative tasks and less on strategic quality improvement.
Low cost of ownership
A modular, cloud-based platform that deploys quickly, scales easily, and eliminates the need for separate BI, ERP, and analytics tools — with a time to value of approximately 8 weeks.
Maintain quality and traceability with a simple workflow
Complex regulatory requirements
From FDA and EMA to ISO and GxP standards, maintaining continuous compliance is resource-intensive and demands consistent documentation, traceability, and audit evidence across all quality processes.
Data silos and inefficient processes
Fragmented documentation across quality, manufacturing, and regulatory teams makes it difficult to ensure data integrity, traceability, and a single source of truth.
Audit readiness
Preparing for inspections and demonstrating end-to-end control over quality events can stall innovation and slow time-to-market when records are scattered across disconnected systems.
Scalability and global operations
As organisations grow, managing quality consistently across multiple sites, partners, and product lines with a platform that lacks deep Salesforce ecosystem integration becomes increasingly limiting.
Limited analytics without additional tools
Quality leaders need real-time insights to drive continuous improvement, but relying on separate BI tools for advanced analytics creates additional cost, maintenance, and data consistency challenges.
No AI to accelerate quality processes
Manual workflows for document creation, CAPA investigation, and risk analysis are slow and error-prone. Without AI assistance, quality teams spend more time on administrative tasks and less on strategic quality improvement.
All-in-one QMS solution managing compliance, quality, and operations
Compliance
Pre-configured workflows and templates aligned with FDA 21 CFR Part 11, ISO 13485, and GxP standards — so your team spends less time building compliance infrastructure and more time on quality outcomes.
Unified Platform
Centralised control of documents, CAPAs, change management, training, audits, manufacturing, TMF, and regulatory submissions — eliminating data silos and reducing the number of systems your team must manage.
Real-Time Visibility
Advanced analytics and dashboards — powered by the Salesforce platform — give quality leaders actionable insights across all quality processes without needing a separate BI tool.
Scalable & Secure
Cloud-based, Salesforce-native architecture designed to grow with your organisation while maintaining strict data security, traceability, and enterprise-grade performance at scale.
Reduced validation effort
Significantly reduced through pre-configured, validation-ready workflows, clear traceability, and a risk-based approach aligned with GxP expectations.
Low cost of ownership
A modular, cloud-based platform that deploys quickly, scales easily, and eliminates the need for separate BI, ERP, and analytics tools — with a time to value of approximately 8 weeks.
See exactly how the two platforms stack up on the criteria that matter most to regulated quality teams.
Comparison based on publicly available product information from both vendors as of May 2026. Features and capabilities may change over time.
Switching is easy.
Migrate from QT9 in 4 simple steps
We analyse your QT9 configuration and map documents, CAPAs, training records, and quality processes to Matrix Quality.
Documents, CAPA records, and training data migrated with full traceability and version history preserved.
Workflows, roles, and templates configured with IQ/OQ/PQ documentation ready for your CSV validation process.
Full onboarding with a dedicated Customer Success Manager from day one.
Thank you
A member of our team will be in contact within 48 hours.
Stop fighting your quality system.
Start shipping safer products.
Join 500+ life sciences companies who chose a smarter path to eQMS.