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DANSK DS/CEN/TR 17223 [ Active ]

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

standard by Dansk Standard , 03/27/2018

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Product Details

Edition:
18
Published:
03/27/2018
Number of Pages:
87
File Size:
1 file , 1.8 MB
Product Code(s):
DS-081, DS-081
 

Document History

  1. DANSK DSF/FPRCEN/TR 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

    • Historical Version

  2. DANSK DS/CEN/TR 17223

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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

    • Most Recent