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Security testing for medical devices includes exploring all avenues of software vulnerabilities and can go far beyond simple vulnerability scanning. Proper testing to address attack surfaces characterized in product threat models requires advanced penetration testing techniques to fully evaluate the cybersecurity of healthcare and medical devices, as shown below.
UL Solutions offers various penetration testing services, from testing aligned with current standards to custom penetration testing, developed to fit your needs. Our penetration tests thoroughly analyze device software functions and components, including hardware.
Our experts work with medical device manufacturers and healthcare providers to assess potential risks related to software weaknesses and vulnerabilities. Our cybersecurity services support efforts to identify, evaluate and address these risks throughout the product life cycle. Connect with us to discuss how we can support your system or product’s security strategy.
Medical device penetration testing is used for more than cybersecurity now. It can address software quality, interoperability and artificial intelligence (AI) risks.
Amendment 524B of the FD&C Act sets new U.S. FDA cybersecurity rules for medical devices. UL Solutions provides expert support to help manufacturers meet these requirements.
Read UL Solutions experts’ responses to medical device manufacturers’ top questions about cybersecurity shared during our two-part webinar series, “Advancing Cybersecure Medical Devices.”
How do we define a “medical cyber device,” and how to confirm medical cyber devices are safe, secure and resilient?
The webinar discusses how stakeholders in the healthcare industry can address today’s top cybersecurity threats.
This on-demand webinar discusses the importance of the total product lifecycle in managing cybersecurity of medical devices, including post-market issues like their end-of-life, end-of-support, decommissioning, and disposal.
This on-demand webinar talks about what it means for a medical device to be a cyber device from the perspective of software risks.
In this webinar, industry experts have shared the importance of medical devices meeting FDA guidelines and third-party cybersecurity standards, ongoing cybersecurity testing, and established threat modeling processes associated.
