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ISO 13485:2016 and ISO 13485:2003 - Medical Devices Transition Set

ISO 13485:2016 and ISO 13485:2003 - Medical Devices Transition Set

ISO 13485:2016 and ISO 13485:2003 - Medical Devices Transition Set provides the latest medical devices quality management system requirements for regulatory purposes. The Medical Devices Transition Set has been designed to be applicable medical device QMS at various stages of the life cycle including design/development, production, storage, distribution, installation, and servicing. ISO 13485:2016 and ISO 13485:2003 - Medical Devices Transition Set also enables for organizations to demonstrate their ability to comply with regulatory requirements regardless of their size and type. ISO 13485:2016 and ISO 13485:2003 - Medical Devices Transition Set supports an organization in need of transitioning their Medical Devices QMS program from ISO 13485:2003 to ISO 13485:2016 by providing both versions of the medical devices quality management systems documents for comparison. The ISO 13485:2016 and ISO 13485:2003 - Medical Devices Transition Set includes:
ISO 13485:2016
ISO 13485:2016 - Medical devices - A practical guide
ISO 13485:2003 (Historical Document)

ISO 13485:2016 and ISO 13485:2003 - Medical Devices Transition Set includes:


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International Organization for Standardization [ISO]


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