The new EU Medical Device Regulation EU MDR 2017/745 with Monir El Azzouzi

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Easy Medical Device

Easy Medical Device

Күн бұрын

Пікірлер: 9
@dhanushpsg5927
@dhanushpsg5927 2 жыл бұрын
Thank you so much
@EasyMedicalDevice
@EasyMedicalDevice 6 жыл бұрын
if you prefer to listen to Medical Device made Easy Podcast on your preferred platform as iTunes, Spotify, Soundcloud... please look at podcast.easymedicaldevice.com
@moonswhite1409
@moonswhite1409 5 жыл бұрын
Thank you very much Very very helpful content :)
@EasyMedicalDevice
@EasyMedicalDevice 5 жыл бұрын
You‘re welcome.
@halaaltayar9448
@halaaltayar9448 5 жыл бұрын
Thank you
@mohammedasif7667
@mohammedasif7667 3 жыл бұрын
Hi Question ; Assume i have a company in Arab and I open up one more plant in Europe so in this do we need Notified body, ec rep distributor, importer ?? Like I manufacturers it and want to deliver to Europe
@EasyMedicalDevice
@EasyMedicalDevice 3 жыл бұрын
Hi Mohammed, If you have a company in Europe then you don‘t need an EC REP or importer. For the Notifief body it depends of the product class. In or out of EU you will need a Notified Body if your product is higher than class I
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