Articles by Editorial Team
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
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.
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4 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
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.
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3 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
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.
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5 min read
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.
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7 min read
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.
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6 min read







