Medical device manufacturers are learning to temper their market enthusiasm with the realities of more connected devices in the field — which means dealing with growing cybersecurity risks.
Fortunately, regulators and policymakers are providing cybersecurity guidance to help medical device manufacturers implement security best practices. The U.S. House of Representatives recently passed new legislation, H.R. 7667, which includes cybersecurity requirements for medical device manufacturers.
In this white paper, we discuss:
- What is H.R. 7667.
- How H.R. 7667 applies to software development.
- Examples of medical device vulnerabilities.
- How SAST tools — like Klocwork — help prevent vulnerabilities and enforce H.R. 7667 guidelines.
To learn more about how to navigate H.R. 7667, download this white paper.