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By adminMy239810
28 juin 2022
Interview

myBrain Technologies’s eye on Medical Device Regulation.

In order to improve health safety and harmonize rules within the EU, the Medical Device Regulation has been profoundly revised, resulting in new regulatory requirements - effective from May 26, 2021. To understand the difficulties of its application by manufacturers and find solutions, we interviewed Sophie Colliot.

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Mark of trust certified ISO 13485 quality management for medical devices white- ogo En GB 1019 1
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