Tame the complexity of your medical digital device development with comprehensive cross-platform tools targeted to each stage of the software delivery and maintenance lifecycle.
Reduce the time-to-market of your medical software, by accessing and customizing production-proven components and functions already in use across a variety of medical devices and regulated industries.
With Qt, you readily get access to a large set of libraries and customizable primitive UI app constructs—among which control elements, menus, but also encryption protocols, secure storage, DICOM view support, among other things—allowing you to shorten time-to-market and inherit out-of-the-box long-term support.
Qt has a strong production history in the medical sector with millions of medical devices built with Qt currently on the market that have passed Class I, Class II and Class III FDA certification and Class I, Class IIa, IIb, and III EU certification. 90% of the top Global MedTech companies build their products with Qt.
Efficiently drive early clinical and human-factor testing with an integrated design-develop-test workflow enabling rapid error detection and quick iterations.
Given the trending shift from hospitalization to home care and the frequent incidents caused by medical device misuse, regulatory bodies insist on the importance of intuitive usability and human factor testing. In addition to the possibility of sharing fully functional prototype applications across teams over the web for UI/UX verification (Qt Design Studio), the Qt product family includes automated QA tooling for early verification of the software functions (Squish), code coverage (Coco), compliance with coding guidelines (Axivion). With Qt Insight, you can validate your product’s functionality to gain direct insights into your application’s actual usage for an out-of-the-box post-market surveillance solution.
Efficiently create intuitive medical software applications that meet the highest safety and reliability industry standards and comply with the requirements set by notified bodies.
Whether you are developing FDA or EU Class II or Class III products such as surgical robots, infusion pumps, patient monitoring systems, or medical imaging applications, Qt provides the technology to build precise, robust, and reliable systems. Qt is ISO 9001:2015 certified with an established Quality Management System. The Qt Safe Renderer is certified to both IEC 62304 - Medical Device Software, Software Lifecycle Processes, and IEC 61508 - Functional Safety of Electrical/Electronic/Programmable Electronic Safety-related Systems.
Transform your healthcare device into a smart device, connected to the Internet of Things, for full operability from home and anywhere in complete security without vulnerability risks.
Qt lets you easily port the familiar smartphone-like user experience to your medical software, to ensure straightforward usage, effortless navigation, and intuitive meaning in the palm of your hand. To help medical device manufacturers satisfy their IEC 62304 requirements and mitigate the risks associated with using software of unknown provenance (SOUP), Qt security-critical code is regularly reviewed, tested, and documented according to cybersecurity industry best practices, including mandatory code reviews, merit-based inspection, continuous integration, and security updates. Being maintained for years with security updates, patches, and a stable roadmap, Qt long-term releases secure your product’s permanence on the market over time.
Transform your healthcare product into a smart device, connected to the Internet of Things, for full operability from home and anywhere in complete security.
When health and well-being are at stake, there can be no compromise on your UI software's quality, safety, and security. Qt provides efficient tooling for designing and implementing effective healthcare UI applications and the extensive, automated testing and post-market surveillance needed to meet the highest certification standards.