This is really amazing. You almost covered all the new changes to EU MDR and can be a great starting point for freshers to understand what is MDR and why it should be and also the part of compliance is explained pretty well. Thanks for the great course amd I know with this many people will get benefited
@pontusgedda2 жыл бұрын
Thank you very much Kumaran! Always glad to see that people are appreciating the job you do. The full course at medicaldevicehq.com is even better. 🙂
@fritzschnitzmueller37682 жыл бұрын
Great short presentation! Thanks for sharing this
@larahamilton22732 жыл бұрын
🤯 I’m new to this world. However, I sense that this is a great summary of what I need to know!
@pontusgedda2 жыл бұрын
Hi Lara, Thanks for the comment. Yes it is a lot to understand in this world. Regards Pontus (the presenter)
@lourdesrosales29422 жыл бұрын
thanks!, this is what I definitely needed for start...
@sandrabieliauskaite60582 жыл бұрын
Very interesting short course! Do you mind to share a reliable link where I could download up to date MDR 2017/745? Thank you!
@mokar08733 ай бұрын
My question is : For medical device class Ir: do they need to have CE marking with notified body code? Or only CE with no code?
@beyzag6366 ай бұрын
Thank you so much for useful explanation and nice tips!
@profskett Жыл бұрын
Thanks for your many interesting and well-presented videos on medical device-related topics! Just wondering, do you plan to make any videos aimed at the UK audience, explaining the difference between applicable medical device regulations in UK vs. EU contexts?
@MedicalDeviceHQ Жыл бұрын
Hi, No plans on digging into UK. The market is too small.