BSI PD CEN/TR 17223:2018

Current Revision
Guidance on the relationship between EN ISO 13485:2016 (Medical devices. Quality management systems. Requirements for regulatory purposes) and European Medical Devices Regulation and In Vitro Diagnostic Medical Devices Regulation

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BSI PD CEN/TR 17223:2018

Guidance on the relationship between EN ISO 13485:2016 (Medical devices. Quality management systems. Requirements for regulatory purposes) and European Medical Devices Regulation and In Vitro Diagnostic Medical Devices Regulation

PUBLISH DATE 2018
PAGES 88
BSI PD CEN/TR 17223:2018

Guidance on the relationship between EN ISO 13485:2016 and EU MDR and IV MDR

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