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 [CURRENT]

PD CEN/TR 17223:2018-03-21

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

German title
Leitfaden zum Zusammenhang zwischen EN ISO 13485: 2016 (Medizinprodukte. Qualitätsmanagementsysteme. Anforderungen für regulatorische Zwecke) und den europäischen Verordnungen über Medizinprodukte und In-vitro-Diagnostika
Publication date
2018-03-21
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Original language
English
Pages
88

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Publication date
2018-03-21
Original language
English
Pages
88
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