Medical Device-Quality Management Systems-Requirements for Regulatory Purposes

1 Scope

This Standard 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 and applicable regulatory requirements. Such organizations can be involved in one or more stages of the life-cycle, including design and development, production, storage and distribution, installation, or serving of a medical device and design and development or provision of associated activities. This standard can also be used by suppliers or external parties that provide product, including quality management system-related services to such organizations.  

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