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ISO 13485 on medical devices and related services testing, conformity with standards and regulations, declaration of eligibility to manufacture medical devices, CE, FDA
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ISO 13485 on medical devices and related services testing, conformity with standards and regulations, declaration of eligibility to manufacture medical devices, CE, FDA

In the heat of the Covid season and will be the demand after Covid with the process of moving production to Vietnam from China, we are consulting and supporting Kim Tin Medical Supplies Co., Ltd (Kinyee Vietnam) to build and take ISO 13485:2016 certification.
This is a standard that specifies requirements for a quality management system to be applied in facilities that provide medical devices and related services to ensure product availability. Meet customer requirements and legal requirements

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