CSA Group Guide to the development and inclusion of safety aspects in International Standards for medical devices ISO/IEC Guide 63:2012

Description
ISO/IEC Guide 63:2012 provides guidance to standards writers on how to include safety aspects in the development of medical device safety standards intended to be used within the risk management framework established in ISO 14971. It expands on the concepts developed in ISO/IEC Guide 51 to include safety-related performance and usability. ISO/IEC Guide 63:2012 is intended to be read in conjunction with ISO/IEC Guide 51 and ISO 14971.
Description
ISO/IEC Guide 63:2012 provides guidance to standards writers on how to include safety aspects in the development of medical device safety standards intended to be used within the risk management framework established in ISO 14971. It expands on the concepts developed in ISO/IEC Guide 51 to include safety-related performance and usability. ISO/IEC Guide 63:2012 is intended to be read in conjunction with ISO/IEC Guide 51 and ISO 14971.

Suppliers

Company
Product
Description
Supplier Links
Guide to the development and inclusion of safety aspects in International Standards for medical devices - ISO/IEC Guide 63:2012 - CSA Group
Toronto, Ontario, Canada
Guide to the development and inclusion of safety aspects in International Standards for medical devices
ISO/IEC Guide 63:2012
Guide to the development and inclusion of safety aspects in International Standards for medical devices ISO/IEC Guide 63:2012
ISO/IEC Guide 63:2012 provides guidance to standards writers on how to include safety aspects in the development of medical device safety standards intended to be used within the risk management framework established in ISO 14971. It expands on the concepts developed in ISO/IEC Guide 51 to include safety-related performance and usability. ISO/IEC Guide 63:2012 is intended to be read in conjunction with ISO/IEC Guide 51 and ISO 14971.

ISO/IEC Guide 63:2012 provides guidance to standards writers on how to include safety aspects in the development of medical device safety standards intended to be used within the risk management framework established in ISO 14971. It expands on the concepts developed in ISO/IEC Guide 51 to include safety-related performance and usability.

ISO/IEC Guide 63:2012 is intended to be read in conjunction with ISO/IEC Guide 51 and ISO 14971.

Supplier's Site

Technical Specifications

  CSA Group
Product Category Standards and Technical Documents
Product Number ISO/IEC Guide 63:2012
Product Name Guide to the development and inclusion of safety aspects in International Standards for medical devices
Unlock Full Specs
to access all available technical data

Similar Products