EU Medical Device Regulation (EU MDR): A Practical Approach
ul.com
EU Medical Device Regulation (EU MDR): A Practical Approach
Learn effective and practical approaches that meet EU medical device regulation (MDR) requirements, and how to update them based on notified body feedback.
Dec 2, 2020
Regulation (EU) 2017/745 Medical Device Regulation
Free Mini-Course EU MDR 2017/745 (Medical Device regulation training)
Free Mini-Course EU MDR 2017/745 (Medical Device regulation training)
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🚨 New Video: Essential Definitions in EU MDR Article 2 🚨 In this episode, we’re diving deeper into the European Medical Device Regulation (EU MDR) 2017/745, focusing on key terms that every regulatory professional should know: 🔹 Generic Device Group – How devices are classified based on similar purposes and technology 🔹 Single-Use Device – Understanding devices designed for one-time use only 🔹 Falsified Device – Recognizing devices that falsely represent their identity or CE marking 🔹 Proc
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