Compliance of EUDAMED Obligations Until its Full Functionality
Regulation (EU) 2017/745 on medical devices (MDR) comprises various articles. Its Article 33 requires European Commission to set up a European database on medical devices “EUDAMED.” This EUDAMED will comprise six different electronic systems that will be designated as “modules.” These modules can facilitate in various places such as: Collation and processing of information under […]