Recent articles
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
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
Explore the key differences between the US FDA and EU MDR approval processes for medical devices, essential for global manufacturers navigating dual compliance.
Learn why leading companies choose Mender
Discover how Mender empowers both you and your customers with secure and reliable over-the-air updates for IoT devices. Focus on your product, and benefit from specialized OTA expertise and best practices.
