Webinars & Webcasts
Life Sciences & Medical Devices
UDI in the EU MDR – How different is it from the US FDA?
In this webinar on "UDI in the EU MDR – How different is it from the US FDA?", speaker Lena Cordie...
European markets pose increasing regulatory language requirements for medical device manufacturers. These regulations force manufacturers to incorporate language translation and localization into global development strategies as individual Member States demand product information in the language of the local user..
If you want to learn more about the areas that will be affected once the new Medical Device Regulation comes into effect, check mdreurope.com
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