Adhering to the necessary regulations associated with medical device design and manufacturing is a challenge. In fact, doing so and still being able to meet accelerating production rates and achieve speed-to-market can, at first glance, appear virtually impossible.

The Siemens PLM Software Integrated Quality solution effectively and efficiently assists medical device companies in the implementation of intelligent manufacturing and design processes. Our Integrated Quality solution provides a platform that allows you to increase quality; reduce risk; create alignment between requirements, product and manufacturing specifications, and production targets; while demonstrating compliance with industry quality standards. The medical devices (MD) catalyst accelerates time-to-value for implementing key elements of our Integrated Quality solution, while providing an environment for swift adoption of future software and technologies.

With ready-made, pre-configured templates for automated workflows, the MD catalyst offers medical device companies the ability to electronically and securely catalogue, manage and utilize design history files (DHFs) and device master records (DMR). This advanced medical device data management system speeds the design and manufacturing processes, while also helping eliminate overall complexity. In practical terms, records become easier to track, access and keep organized.