Forcing your developers to work with ancient, legacy tools is like forcing them to wash dishes by hand in a five-star restaurant. And, constantly buying different tools to solve disconnected pieces of the MedTech design and development process creates expensive silos and only heightens the tension between Quality and Operations professionals as they struggle to find and organize necessary information across disconnected systems.

Ketryx doesn’t replace your QMS or documentation system. Rather it frees developers to continue to work in their beloved cloud environments while outputting FDA-ready reports to regulatory professionals that can be stored in existing Quality and documentation systems. Enjoy full support for AWS, Jira, Github, and xx, among others, eliminating the need for complex integrations.

Ketryx reports directly out of your source code, automatically identifying and ranking risk factors for cybersecurity vulnerabilities as well as other potential issues that could result in errors, making them easy to resolve before they affect performance. Spend less resources and time to optimize your quality and design processes while gaining efficiency.

Instead of worrying about compliance or if the process was “done right,” Quality professionals can focus on discovering new insights into any process bottlenecks to enable teams to master their process for the long run. Powered by AI, Ketryx predictive analytics give your company visibility into all areas of your device design and manufacturing process.