Welcome to our informative video on the European Union Medical Device Regulation (EU MDR). In this video, we demystify the EU MDR, explaining its significance in the world of medical devices and healthcare.
📄 Read the EU MDR: For more detailed information on the EU MDR, you can access the full regulation here: [ Ссылка ]
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ISO 13485 is a recognized international standard for medical device quality management systems. Under the EU MDR, medical device manufacturers must establish and maintain a quality management system.
👉 If you would like to become a ISO 13485:2016 Internal Auditor consider taking our auditing course.
This course is delivered via ZOOM (LIVE Virtual Training): hthttps://bit.ly/3WmGLkk
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👉 If you want to learn more about ISO 13485:2016 process, consider taking one of our courses. We offer flexible delivery methods.
ISO 13485:2016 courses delivered via ZOOM (LIVE Virtual Training): [ Ссылка ]
In-Company ISO 13485:2016 courses: [ Ссылка ]
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FREE RESOURCES FOR MEDICAL DEVICE MANUFACTURERS
🔔 FREE EBOOK 🔔
Get it here 👉 [ Ссылка ]
Learn about the Medical Device Single Audit Program (MDSAP) by downloading this FREE ebook. Don't miss it!
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