Promoting international collaboration on AI for medical devices and seeking your input on the newly released draft document “Good machine learning practice for medical device development – Guiding Principles” by the International Medical Device Regulators Forum (IMDRF). Appreciate the many countries that contributed: https://lnkd.in/eRmdwwWd Please provide comments by Aug 30: https://lnkd.in/e4hGh89j #healthcare #AI
Matthew Diamond, MD, PhD’s Post
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Principles of Good Machine Learning Practices for Medical Device Development For my colleagues in the AI/ML space, IMDRF (International Medical Device Regulators Forum) has opened comments on their 10 principles of Good Machine Learning Practices for Medical Device Development. https://lnkd.in/e5xmYRx4
Good machine learning practice for medical device development - Guiding Principles
imdrf.org
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Clinical decision support, medical devices, and AI: Attorney Bradley Merrill Thompson, RAC, discusses these topics, plus regulatory issues and more, in an interview with Xenophon Papademetris for Yale Online's Certificate Program on Medical Software and Medical AI. 🔗 Watch now: https://bit.ly/3vCyUaK #FDA #MedicalDevices #ArtificialIntelligence
Bradley Merrill Thompson Discusses Clinical Decision Support, Medical Devices, and AI in Yale Video
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📣 Attention AI/ML developers, manufacturers and RA interested scrollers!!! New IMDRF document on "Good machine learning practice for medical device development - Guiding Principles" is now open for public consultation. We have been trying our very best to ensure that the most essential parts of creating a solid machine learning-enabled medical device are captured, but in case we missed anything, please let us know using the commenting template. Consultation closes on the 30th of August, so make sure to submit your comments before and enjoy the summer. 📅 🌞
Good machine learning practice for medical device development - Guiding Principles
imdrf.org
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Product Specialist helping Life Science companies digitalise quality processes and excell in compliance regulations with a Smart QMS solution💫
Meet Smarty, Scilife's Medical Device assistant powered by AI 🖥🧠 Smarty's data bank is stored with regulatory knowledge from the Medical Device industry to answer any queries you have. For instance, see what Smart has to say about: 🎯 What is the difference between 21 CFR 820 and ISO 13485? 🎯How should I conduct a management review according to ISO 13485? 🎯 What do I need to do if I want to develop a class II medical device? Try it out here: https://lnkd.in/dVft9_jN
Medical Device Chatbot powered by AI
scilife.io
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Guidance: Software and artificial intelligence (AI) as a medical device https://lnkd.in/gRQz-mdd Information for manufacturers, healthcare professionals, researchers and patients on software as a medical device (SaMD) and AI as a medical device (AIaMD).
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Did you know? 🤔 In a document prepared by the TÜV AI.LAB, we find the abbreviation AIMDSW, which stands for Artificial Intelligence in Medical Device Software. Although AIMDSW is not yet commonly used, it’s worth remembering this abbreviation as the number of usage of AI in healthcare grows. Get to know more about AI Act in medical software development from our blog https://bit.ly/463iHJP #aisoftware #medai #healthcareai #medicalsoftware #samd
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Chil Femtech Center introduces KETI 4.0, an AI Companion designed to assist in comprehending medical records. This groundbreaking tool enables users to input medical text, receiving simplified explanations in their preferred language. KETI does not substitute professional medical advice; it serves as a supplementary resource. Expert guidance remains paramount. https://lnkd.in/dKvTTDCD
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Please join us for a webinar on "The Impact of the EU AI Act on Medical Devices and IVDs." The webinar will explore the impact of the AI Act on medical devices and IVDs, including an overview of the obligations that will apply to providers and deployers of relevant medical devices/IVDs, and detail on the timelines for compliance with the new rules.
Medical Device Webinar Series | The Impact of the EU AI Act on Medical Devices and IVDs
event.on24.com
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AI Product Management | Gen AI | AI for Medical Imaging | Computer Vision | Med Tech | Regulatory | Global Product Lead | Department Manager |
🔍 EU AI Act <> MedTech Webinar Alert 🔍 With the EU AI Act officially adopted, MedTech companies building AI products must navigate new regulations. Join this insightful webinar on how the AI Act impacts the medical device industry. 🎙️ 📅 Date: May 30th 2024 🕒 Time: 16:00 - 17:00 Irish Time 📍 Register Here: https://lnkd.in/d4MUR4mf Expert speakers from industry, legal, and notified body TÜV SÜD will delve into: 📊 The gap between current compliance and the AI Act's requirements 🛠️ Real-world challenges manufacturers will face 🔎 The new combined conformity assessment procedure 📁 Practical implications focusing on data and documentation requirements #MedTech #AIAct #Webinar #MedicalDevices #Compliance #Regulations #AI #Innovation
Webinar: What the AI Act Means for Medical Devices
mhc.ie
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