Articles by Editorial Team

    New Mender experimental AI-enabled feature

    New Mender experimental AI-enabled feature

    Discover Mender's new experimental AI feature that simplifies failure analysis for IoT device updates, saving time and effort for hosted Mender users.
    Mender in 2025: Preparing for Compliance, Security, and AI-Driven Growth

    Mender in 2025: Preparing for 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.
    What’s new in Mender: Enhanced delta updates and user experience

    What’s new in Mender: Enhanced delta updates and user experience

    Discover Mender's latest enhancements in delta updates and user experience, including server-side delta generation and user-friendly subscription management, in our newest product release.
    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.
    Why OTA updates are now mission critical for future-proofed device lifecycle management

    Why OTA updates are now mission critical for future-proofed device lifecycle management

    Discover why Over-The-Air (OTA) updates are essential for future-proofing IoT device lifecycle management, ensuring security, compliance, and continuous improvement in an evolving technological landscape.
    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.
    New Mender packaging and distribution channels

    New Mender packaging and distribution channels

    Simplify installing and updating Mender with new apt repositories, improving security, dependency handling, and version control.
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