CSA - CAN/CSA-ISO 13485-03
Medical devices - Quality management systems - Requirements for regulatory purposes
inactive
| Organization: | CSA |
| Publication Date: | 1 December 2003 |
| Status: | inactive |
| Page Count: | 72 |
| ICS Code (Quality management and quality assurance): | 03.120.10 |
| ICS Code (Medical equipment in general): | 11.040.01 |
Document History
January 1, 2016
Medical devices - Quality management systems - Requirements for regulatory purposes
This International Standard specifies requirements for a quality management system where an organization needs to demonstrate its ability to provide medical devices and related services that...
December 1, 2003
Medical devices Quality management systems Requirements for regulatory purposes
General
This International Standard specifies requirements for a quality management system where an organization needs to demonstrate its ability to provide medical devices and related services that...
CAN/CSA-ISO 13485-03
December 1, 2003
Medical devices - Quality management systems - Requirements for regulatory purposes
A description is not available for this item.
December 1, 2003
Medical devices - Quality management systems - Requirements for regulatory purposes
General
This International Standard specifies requirements for a quality management system where an organization needs to demonstrate its ability to provide medical devices and related services that...
January 1, 1998
Quality Systems - Medical Devices - Particular Requirements for the Application of ISO 9001
This International Standard specifies, in conjunction with ISO 9001, the quality system requirements for the design/development, production and, when relevant, installation and servicing of medical...