Historical

ANSI/AAMI/ISO 13485:2016

Medical devices - Quality management systems - Requirements for regulatory purposes.


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 related services.


CONTENT PROVIDER
Association for the Advancement of Medical Instrumentation [aami]

Others Also Bought
Quality management systems - Requirements
Guidelines for auditing management systems
CONSOLIDATED TEXT - Medical device software - Software life cycle processes
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Amendments & Corrections
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