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.
Author: Antònia Escales Oliver
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.
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.
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.