This certification recognizes the effort made by our company in updating its Quality Management System to the new requirements of the Medical Devices regulations.

The work done does not stop there. With the entry into force of the new Regulation (EU) 2017/745 on Medical Devices, we are in a position to adapt to the new requirements of medical devices manufacturers. With the new ISO 13485:2016 certificate we are taking a further step towards the more demanding compliance required for products manufactured by C.V. Médica, S.L.

Quality Department

ISO 13485: 2016 Medical devices. Quality management systems.

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