ISO 13485: 2016 Medical Devices

ISO 13485 specifies requirements for a Quality Management System for organisations required to demonstrate its ability to provide medical devices that consistently meet client and regulatory requirements.
ISO 13485 is the most accepted global standard of its kind and will bring your business a host of benefits, including:
* Full ISO 13485 compliance - which is fast becoming a prerequisite for regulatory authorities everywhere* ISO 13485 will establish robust development, manufacture, distribution and control processes* ISO 13485 will also help you to monitor your supply chain so that you are always in control* The standard will help to optimise efficiency and minimise costs*Be confident that your company has a quality system that meets the demands of legislation in every corner of the global market.

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