Historical

ANSI/AAMI/ISO 13485-2003

Quality Management Systems - Medical Devices - System Requirements for Regulatory Purposes


Specifies requirements for a quality management system where an organization needs to demonstrate its ability to provide medical devices that consistently meet customer requirements and regulatory requirements applicable to medical devices.


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

Others Also Bought
Medical devices - Application of risk management to medical devices (and amendment)
Medical devices - Quality mangement systems - Guidance on the application of ISO 13485: 2003
Quality systems-Medical devices-Guidance on the application of ISO 13485 and ISO 13488, 1ed
Document History
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