Amid the ongoing pandemic, groups like the European Commission (EC) and the International Accreditation Forum (IAF) have announced notified bodies (NBs) can conduct remote audits for key [...]
Blog Home TAG: EU MDR
Join us for a one-hour webinar focused on efficient management of postmarket challenges faced by medical device manufacturers marketing devices in the EU. DATE: Tuesday, February [...]
By Tony ParisePosted
In four months, the new EU Medical Device Regulation (MDR) goes into effect, which officially means it’s crunch time for devices that need to be certified to the new law. What should companies be [...]
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