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CSA - CAN/CSA-ISO 13485-98

Quality Systems - Medical Devices - Particular Requirements for the Application of ISO 9001

inactive
Organization: CSA
Publication Date: 1 January 1998
Status: inactive
Page Count: 21
scope:

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 devices.

This International Standard, in conjunction with ISO 9001, is applicable when there is a need to assess a medical device supplier's quality system.

As part of an assessment by a third party for the purpose of regulatory requirements, the supplier may be required to provide access to confidential data in order to demonstrate compliance with this International Standard. The supplier may be required to exhibit these data but is not obliged to provide copies for retention.

NOTE - In this International Standard the term "if appropriate" is used several times. When a requirement is qualified by this phrase, it is deemed to be "appropriate" unless the supplier can document a justification otherwise. a requirement is considered "appropriate" if its non-implementation could result in

- the product not meeting its specified requirements, and/or

- the supplier being unable to carry out corrective action.

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
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...
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 13485-98
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...

References

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