Category
IOT & OTA
Succeeding in the IoT product landscape: How OEMs align AI, software, and time-to-Market
Discover how OEMs can effectively align AI and software to enhance their IoT products, tackle time-to-market challenges, and ensure long-term success.
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4 min read
What’s new in Mender: New Update Modules for container updates
Discover Mender's new Update Modules for OTA container updates, enhancing deployment efficiency and network reliability for seamless software updates.
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3 min read
Beyond traditional connectivity: managing smart products and machines in air-gapped and offline environments
Explore how to manage smart devices in air-gapped and offline environments with secure, authenticated software updates, ensuring compliance and operational efficiency.
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7 min read
Key considerations: How to build compliant software update practices for medical devices
Learn how to implement compliant software update practices for medical devices while navigating FDA and EU MDR regulations, ensuring safety and cybersecurity.
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7 min read
Mender Client 6.0 released
Discover the new features in Mender Client 6.0, including official Docker Compose support and enhanced network robustness for reliable IoT device updates.
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2 min read
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.
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4 min read
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.
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3 min read
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.
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5 min read
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.
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6 min read







