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PD CEN/TR 17223:2018

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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

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Author BSI
Editor BSI
Document type Standard
Format File
EAN ISBN 978 0 580 51912 3
ICS 11.040.01 : Medical equipment in general
03.100.70 : Management systems
Number of pages 88
Cross references CEN/TR 17223:2018 IDT
Set MYSTD-20STD
Year 2018
Country UK