Classification of Medical Devices - EU 2017/745

🔍 Dive into the intricate world of medical device classification under the European Medical Device Regulation (MDR) 2017/745 🏥
In this video, we break down the key aspects of MDR 2017/745, providing a clear and concise overview of the classification process for medical devices. Whether you're a healthcare professional, regulatory affairs specialist, or simply curious about the intricate regulatory landscape, this video is tailored for you.
💡 Why Watch?
- Gain a deep understanding of the classification criteria for medical devices.
- Navigate the regulatory landscape with confidence, ensuring compliance with MDR 2017/745.
- Learn about the responsibilities of manufacturers, distributors, and the role of Notified Bodies.
- Stay informed about the transition period and key deadlines.
👩‍⚕️ Who Should Watch?
- Healthcare professionals
- Medical device manufacturers
- Regulatory affairs specialists
- Quality assurance professionals
- Anyone interested in the regulatory framework for medical devices in the European Union.
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Thank you for tuning in! Let's unravel the complexities of MDR 2017/745 together. 💉🔬🔒 #MedicalDeviceRegulation #MDR2017745 #HealthcareCompliance