In today’s landscape of increasingly connected devices, the fusion of healthcare and technology offers transformative opportunities in patient care. However, this digital evolution also opens a Pandora’s box of cybersecurity vulnerabilities, particularly in medical devices. Recognising this pressing issue, the US Food and Drug Administration (FDA) recently issued new regulations aimed at mitigating these risks. This action elevates cybersecurity to a central position in the manufacturing and management of medical devices.
Let’s take a comprehensive look back at our 17 August webinar, where we explored the FDA’s new regulations on medical device cybersecurity.