Customer Service:
Mon - Fri: 8:30 am - 6 pm EST

 Historical

ISO/TR 14969:2004

Medical devices - Quality mangement systems - Guidance on the application of ISO 13485: 2003

ISO/TR 14969:2004 provides guidance for the application of the requirements for quality management systems contained in ISO 13485. It does not add to, or otherwise change, the requirements of ISO 13485. It does not include requirements to be used as the basis of regulatory inspection or certification assessment activities.

This guidance can be used to better understand the requirements of ISO 13485 and to illustrate some of the variety of methods and approaches available for meeting the requirements of ISO 13485.


Content Provider
International Organization for Standardization [iso]


Others Also Bought

Medical devices - Quality management systems - Requirements for regulatory purposes
Medical devices - Application of risk management to medical devices
Quality Management Systems - Medical Devices - System Requirements for Regulatory Purposes
Document History
Revises:
Revised By:
Amendments & Corrections
We have no amendments or corrections for this standard.
ANSI Logo

As the voice of the U.S. standards and conformity assessment system, the American National Standards Institute (ANSI) empowers its members and constituents to strengthen the U.S. marketplace position in the global economy while helping to assure the safety and health of consumers and the protection of the environment.

CUSTOMER SERVICE
NEW YORK OFFICE
ANSI HEADQUARTERS