Medical device software development must consider cybersecurity from the design stage to protect patient safety and data privacySecurity should be integrated early in the development lifecycle, not added as a separate component laterCyber threats to medical devices can lead to compromised treatment settings, vital signs, or data transmissionConsiderations such as user authentication, data encryption, and access controls are crucial for mitigating risks in medical softwareIEC 62304 standard provides guidelines for secure development processes, emphasizing documentation, traceability, and verificationStructured risk analysis helps identify threats, assess likelihood, and determine consequences, guiding the selection of security controlsCoordination among development, quality assurance, regulatory, and clinical teams is essential for effective cybersecurity implementationDevices should be designed for flexibility, with secure update mechanisms and monitoring systems for anomaly detectionCybersecurity in medical device software is about proactive design for resilience and trust, not just meeting compliance standardsSecure-by-design is a necessary standard to build products that can be trusted in critical clinical scenarios