QT9 Software, a global technology leader in Quality Management Software, ERP, and MRP solutions, will exhibit at MD&M West 2026, taking place February 3–5, 2026, in Anaheim, CA. At booth 3279, QT9 Software will showcase its QT9 QMS, a quality management platform designed to empower organisations in life sciences, medical device, and biotechnology manufacturing with streamlined quality processes, automated compliance workflows, and simplified ISO and FDA requirements, all in a single, integrated system says the company.
QT9 QMS offers a cloud-based deployment model, eliminating installation hassles and providing instant access via any web browser or operating system. Teams benefit from free software maintenance, continuous updates, multi-site readiness, and unlimited training to ensure rapid implementation and reliable system performance.
Export options and drill-down functionality provide actionable insights for fast, informed decision-making. At MD&M West, visitors will see how these real-time analytics and reporting capabilities help medical device quality and regulatory teams respond faster to issues and audits.
QT9 QMS centralises document control, supporting structured document review, secure storage, revision tracking, and effortless sharing with unlimited internal and external users. Its robust quality assurance suite includes defect tracking, incident management, equipment and supplier quality monitoring, and ERP integration, enhancing operational reliability and fostering continual improvement.
QT9 QMS is delivered prevalidated, including IQ (Installation Qualification), OQ (Operational Qualification), and PQ (Performance Qualification) protocols, enabling rapid deployment and audit-readiness out of the box for regulated medical devices and other life sciences environments.
Compliance automation is at the core of QT9 QMS, simplifying regulatory requirements through electronic signature approvals, automatic audit trails, revision control, and validation protocols. The system is pre-validated for ISO 13485, FDA 21 CFR Part 820, and EU MDR, ensuring rapid and reliable implementation for audit readiness and regulatory peace of mind in the medical device sector.
Upskilling and employee training are made easy with integrated modules for assessment management, assignment allocation, course tracking, self-learning, and tests and quizzes. Built-in web portals provide secure, dedicated access for customers, employees, and suppliers, promoting transparent communication and collaboration within regulated supply chains serving the medical device and broader life sciences industries.
The company says QT9 QMS delivers all the tools necessary for organisations to connect quality with people, drive customer satisfaction, improve accuracy, accelerate productivity, and adapt quickly to changing market or regulatory demands in medical devices and related life sciences manufacturing.
