[PDF.00re] ISO 13485:2003, Medical devices - Quality management systems - Requirements for regulatory purposes
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ISO 13485:2003, Medical devices - Quality management systems - Requirements for regulatory purposes
ISO/TC 210
[PDF.zc18] ISO 13485:2003, Medical devices - Quality management systems - Requirements for regulatory purposes
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| #4595627 in Books | 2011-05-03 | 10.50 x.16 x8.20l, | File type: PDF | 66 pages|
ISO 13485:2003 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.
The primary objective of ISO 13485:2003 is to facilitate harmonized medical device regulatory requirements for quality management systems. As a result, it includes som...
You can specify the type of files you want, for your device.ISO 13485:2003, Medical devices - Quality management systems - Requirements for regulatory purposes | ISO/TC 210. A good, fresh read, highly recommended.