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List of Notified bodies accredited for CE Certification

A notified body is an organization that has been accredited by an EU Member State to conduct a conformity assessment under the relevant EU Directives and issue CE certificate. After certification manufacturers can affix CE Mark on their Medical device and are free to market their devices in all EU Member states. Manufacturers can choose any notified body for conformity assessment (audit

ISO 13485 Certification What Is the ISO 13485 Standard?

ISO 13485 contains requirements that are essential for any organization operating at any tier in the medical device and pharmaceutical supply chain. ISO 13485 certification is especially relevant to manufacturers that wish to demonstrate applicable regulatory requirements, and by organizations whose services support medical device manufacturers.

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ISO 13485 Certification What Is the ISO 13485 Standard?

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TÜV SÜD certification marks and certificates represent third party endorsement by a globally renowned organisation. It is a mark of distinction that serves as excellent marketing tools, enhancing the value of your brand and inspiring greater confidence among your business partners and end users.

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