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QT9 Software Blog

See How QT9 QMS Transforms Medical Device Compliance at MD&M West

QT9 QMS at Booth 3279 at MD&M West in Anaheim.
See How QT9 QMS Transforms Medical Device Compliance at MD&M West
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QT9 Software, is exhibiting at MD&M West 2026, February 3–5, 2026, at the Anaheim Convention Center, bringing its robust QT9 QMS platform to medical device and life sciences manufacturers looking to modernize quality management and simplify compliance.​

Transforming quality at MD&M West

At MD&M West 2026, QT9 Software will showcase QT9 QMS at booth 3279, highlighting how one integrated system can help medical device, biotechnology and broader life sciences manufacturers streamline quality processes, automate compliance workflows and simplify ISO and FDA requirements. The cloud-based platform gives teams instant access through any web browser or operating system, with free maintenance, continuous updates, multi-site readiness and unlimited training that supports rapid implementation and long-term reliability.​

Automated, integrated quality management

QT9 QMS is designed to eliminate the complexity of fragmented systems by centralizing critical quality activities in one place. From to-do lists, email alerts, user-defined fields and permission controls to integrated defect tracking, incident management, equipment and supplier quality monitoring, and ERP integration, teams can manage quality and operations in a unified environment that supports continual improvement.​

Real-time visibility for faster decisions

Dynamic reporting capabilities within QT9 QMS give organizations real-time visibility into quality and compliance data, with timeline traceability and personalized dashboards that make it easier to analyze performance and identify trends. Powerful filtering, sorting, graphical presentations, export options and drill-down functionality provide actionable insights so quality and regulatory teams can respond faster to issues and audits.​

Built-in compliance and validation

Compliance automation sits at the core of QT9 QMS, with prevalidated IQ, OQ and PQ protocols that support rapid deployment and audit-readiness out of the box for regulated medical device and life sciences environments. The system supports electronic signature approvals, automatic audit trails, revision control and validation protocols, and is pre-validated for standards including QMSR, ISO 13485, ISO 9001 and EU MDR, helping manufacturers maintain regulatory peace of mind.​

Empowering teams, suppliers and customers

QT9 QMS also helps organizations upskill their workforce with integrated training modules for assessment management, assignment allocation, course tracking, self-learning, and tests and quizzes. Built-in web portals offer secure access for customers, employees and suppliers, improving communication and collaboration across regulated supply chains in the medical device and broader life sciences industries.​

Flexible deployment for growing manufacturers

To meet regional and organizational requirements, QT9 offers flexible deployment options, including cloud or on-premise hosting, with data residency choices in the United States or European Union. Additional capabilities, such as automated CAPA management, streamlined audit scheduling, deviation monitoring, risk minimization, complaint and feedback tracking, inspection management, engineering change control with electronic approvals, and a comprehensive training environment help manufacturers support job-specific compliance at scale.​

Supporting continuous improvement in regulated industries

Manufacturers using QT9 QMS can streamline device history record management, design and development workflows, and compliance documentation to stay inspection-ready while driving continuous improvement. With an integrated, scalable platform purpose-built for regulated industries, QT9 Software helps organizations connect quality with people, improve accuracy, drive customer satisfaction, and adapt quickly to changing market and regulatory demands in medical devices and related life sciences manufacturing.​

To see QT9 QMS in action at MD&M West 2026, visit QT9 Software at booth 3279 or learn more and schedule a personalized demo at www.qt9software.com/qms/demo.

More than just software—a partner in growth

QT9 Software has been a trusted partner for thousands of businesses worldwide, providing innovative solutions that improve efficiency and ensure the quality and safety of their products. QT9 Software empowers thousands of the world’s best brands to ensure the quality and safety of their products and services through its QMS, ERP and MRP software, as well as complementary solutions. For more information, visit the QT9 Software website at https://qt9software.com.