News
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Medical Devices: Have your say on the EU rules!
The EC has initiated a public consultation to assess the effectiveness, efficiency, relevance, and coherence of the EU regulations on medical devices (Regulation 2017/745) and in vitro diagnostic devices (Regulation 2017/746). This is a key opportunity for stakeholders to help shape the future of medical device regulations in Europe, ensuring that they continue to prioritize patient safety while supporting innovation.
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PhD and postdoc opportunities - December 2024
New calls with deadlines end December - early January
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EDITH-CSA is wrapping up the Virtual Human Twin roadmap
The policy brief of the VHT roadmap is open for public consultation. This is your last chance to provide input and feedback, donβt miss it!
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A heartfelt thank you to the YSC
The current committee is ending a 2-year mandate in December while new applicants will be selected soon
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In the literature: November 2024 highlights
Click here to read some interesting recently published papers from our community. If you have published an article in the field of in silico medicine, send it to us: we will include it in this section of the newsletter!
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Medical devices AI questionnaire jointly published by IG-NB & Team NB
A position paper and questionnaire were recently published regarding the applicability of Artificial Intelligence (AI) in medical devices under MDR and IVDR regulations.
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