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Standards [CURRENT]

PD CEN/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

Title (German)

Leitfaden zum Zusammenhang zwischen EN ISO 13485: 2016 (Medizinprodukte. Qualitätsmanagementsysteme. Anforderungen für regulatorische Zwecke) und den europäischen Verordnungen über Medizinprodukte und In-vitro-Diagnostika

Edition 2018-03-21
Original language English
Price from 403.40 €
Table of contents