ebook

Securing medical device software reliability

Woman checking glucose levels on smart phone from a small, wireless device attached on her arm.

Software reliability is essential for medical device embedded software due to the rise in connected devices. Cyber threats, data protection requirements, post-release updates and the incorporation of modern technologies like AI and machine learning have added complexity to device software, raising the potential for device failures and scrutiny from regulatory bodies. Manufacturers can efficiently navigate these hurdles with the help of our designed embedded Linux solutions and Connected Care software reliability tools.

Integrated tools for reliable medical device software development

Our Connected Care software reliability tools cover various platforms, offering a comprehensive security process that tracks, evaluates and rectifies critical security flaws. These tools monitor vulnerabilities, provide patches and reduce Linux usage risks for safety-certified medical devices. They also support IoT connectivity, multiple cloud platforms and real-time operating systems (RTOS), outlining development, reducing costs and enabling robust, secure systems. We empower users to streamline regulatory compliance, accelerate time-to-market, minimize risk, and implement IoT and cloud strategies, ultimately fostering efficient, reliable and secure medical devices.

Download the ebook to learn more about our Connected Care software reliability tools.

You might also be interested in…

SaaS Enterprise Recipe Management

Implementing Enterprise Recipe Management offers several benefits, including accelerated innovation, improved collaboration, better understanding of the impact of decisions, increased productivity, and faster speed to market.

Read blog

The past decade has seen a surge in devices connected to the internet, offering numerous benefits but raising concerns about security issues like password vulnerabilities and ransomware incidents. Medical device security is crucial for assuring customers and patients their health and personal information are protected. The FDA provides guidance focusing on cybersecurity, covering device design, labeling, documentation and post-market management. We’ll take a look at software development, maintenance and using off-the-shelf software in medical devices, addressing vulnerabilities, prevention, mitigation and post-release actions. These recommendations are applicable not just to the United States but also to other regulatory bodies worldwide seeking approval for medical devices.

Securing medical device software reliability

Integrated tools for reliable medical device software development

Share