Blog Security Safeguard Medical Devices: New H-ISAC Guidance on Cusp of FDA Rule Carley Thornell is a former Industry Marketing Strategist for Healthcare and Life Sciences at Akamai. She has a deep background in thought leadership in the technology space, including leading the content strategy and research team at one of the country’s leading electronic health records systems. The fourth quarter is notable across the healthcare ecosystem for myriad reasons. Payers have their peak season of open enrollment, and providers race to complete annual exams for their patient panels.  \r\n In the HCIT sector, autumn 2023 also brings an important milestone: Beginning October 1, the US Food and Drug Administration (FDA) will exercise its authority to refuse medical device manufacturers’ premarket submissions if they do not include cybersecurity software and update capabilities. \r\n It’s about time.…