ISO 13485

BS EN ISO 13485 – 2016 is designed to be used by organizations involved in the design, production, installation and servicing of medical devices and related services. It sets out the requirements for a quality management system specific to the medical devices industry. By achieving third-party certification CPI have demonstrated to regulators that our quality management processes ensure best practice in everything they do. 

Medical Devices management standards help us to achieve the non-negotiable safety and quality regulatory requirements.

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