PD-CEN-17223 › 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
PD-CEN-17223
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2018 EDITION
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CURRENT
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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
Keywords
Management;Diagnostic equipment (medical);Quality management;Medical equipment;Information management
To find similar documents by classification:
11.040.01 (Medical equipment in general)
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Document Number
PD CEN/TR 17223:2018
Revision Level
2018 EDITION
Status
Current
Publication Date
March 21, 2018
Page Count
88
ISBN
9780580519123
International Equivalent
CEN/TR 17223:2018
Committee Number
CH/210