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IOT & OTA

    Complying with the US FDA and EU MDR requires software updates

    Complying with the US FDA and EU MDR requires software updates

    Ensuring compliance with US FDA and EU MDR for connected medical devices requires effective software updates, robust risk management, and thorough documentation throughout the product lifecycle.
    IoT in 2026: Edge AI, growing complexity, and the demand for smarter updates

    IoT in 2026: Edge AI, growing complexity, and the demand for smarter updates

    Explore the key trends shaping IoT in 2026, including Edge AI, hardware complexity, RTOS adoption, and the rise of AI-driven subscription models.
    Mender in 2025: A year in review with compliance, security, and AI-driven growth

    Mender in 2025: A year in review with compliance, security, and AI-driven growth

    A look at how regulatory compliance, security requirements, AI-driven scale, and OTA updates shaped device software management across the Mender ecosystem in 2025.
    Failed lifecycle management is unacceptable in FDA and MDR compliance

    Failed lifecycle management is unacceptable in FDA and MDR compliance

    Ensure medical device compliance with FDA and EU MDR by adopting a lifecycle management strategy from design to post-market, focusing on continuous oversight and improvement.
    The struggle to reach global markets for medical device manufacturers: The importance of international compliance

    The struggle to reach global markets for medical device manufacturers: The importance of international compliance

    Navigating global regulatory compliance is crucial for medical device manufacturers. Learn strategies for documentation, software updates, and post-market surveillance to ensure international success and patient safety.
    The differences between the US FDA’s device approval process and the EU’s medical device regulation (MDR): An essential dual-compliance framework for global manufacturers

    The differences between the US FDA’s device approval process and the EU’s medical device regulation (MDR): An essential dual-compliance framework for global manufacturers

    Explore the key differences between the US FDA and EU MDR approval processes for medical devices, essential for global manufacturers navigating dual compliance.
    The critical role that security and safety requirements play in software-driven medical devices

    The critical role that security and safety requirements play in software-driven medical devices

    Navigating the complexities of security and regulatory compliance in software-driven medical devices to ensure patient safety and innovative advancements in healthcare technology.
    Zephyr RTOS: Accelerating edge IoT products

    Zephyr RTOS: Accelerating edge IoT products

    Discover how Zephyr RTOS accelerates edge IoT product development with robust security, scalability, and resource efficiency, making it a top choice for smart, connected products.
    Engineering robust remote software delivery for embedded systems

    Engineering robust remote software delivery for embedded systems

    Manage OTA updates for embedded systems securely and efficiently with Mender's robust platform, ensuring seamless firmware delivery, system stability, and compliance for diverse industries.
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