

ISO 13485 specifies requirements for a quality management system, where an organization needs to demonstrate its ability to provide medical devices and related services that consistently meet customer requirements and regulatory requirements applicable to medical devices and services. It is the only standard internationally used by medical device manufacturers. The implementation of ISO 13485 allows the reduction of risks for companies that manufacture or supply medical devices and related services at all stages of implementation.
Upon the certification process successfully completed, SRAC certified organizations:
Every successful organization should:
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