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Entering the extension period for MDD legacy devices in the EU
Explore how the EU’s extension for MDD legacy devices impacts manufacturers, ensuring compliance with MDR regulations & preventing shortages
Sep 8, 20243 min read
Understanding the vital role of standards in the medical device field
Discover the impact of standards on medical devices, from compliance and safety to global communication and operability.
May 21, 20245 min read
CFR Title 21: Navigating the Landscape of the US Regulatory Framework for Medical Devices
Understand US medical device regulations through CFR Title 21 and how we ensure compliance for innovation and patient safety.
Mar 19, 20243 min read
EU Regulatory Framework for Medical Devices: An Introduction to MDR
Dive into the EU Regulatory Landscape for Medical Devices with this Introduction to MDR. Explore its scope, history, and requirements.
Oct 24, 20234 min read
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