BSI - BS EN ISO 13485 + A11
Medical devices - Quality management systems - Requirements for regulatory purposes
active, Most Current
| Organization: | BSI |
| Publication Date: | 31 March 2016 |
| Status: | active |
| Page Count: | 90 |
| ICS Code (Quality management and quality assurance): | 03.120.10 |
| ICS Code (Medical equipment in general): | 11.040.01 |
| ICS Code (Management systems): | 03.100.70 |
Document History
March 31, 2016
Medical devices - Quality management systems - Requirements for regulatory purposes
A description is not available for this item.
BS EN ISO 13485 + A11
March 31, 2016
Medical devices - Quality management systems - Requirements for regulatory purposes
A description is not available for this item.
March 31, 2016
Medical devices - Quality management systems - Requirements for regulatory purposes
A description is not available for this item.
March 31, 2016
Medical devices - Quality management systems - Requirements for regulatory purposes
A description is not available for this item.
February 29, 2016
Medical devices - Quality management systems - Requirements for regulatory purposes
A description is not available for this item.
March 31, 2012
Medical devices - Quality management systems - Requirements for regulatory purposes
A description is not available for this item.
March 31, 2012
Medical devices - Quality management systems - Requirements for regulatory purposes
A description is not available for this item.
July 24, 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...
July 24, 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...
July 24, 2003
Medical devices - Quality management systems - Requirements for regulatory purposes
A description is not available for this item.
March 15, 2001
Quality Systems - Medical Devices - Particular Requirements for the Application of EN ISO 9001
To be read in conjunction with BS EN ISO 9001:1994