WHO Global Model Regulatory Framework for Medical Devices including IVD medical devices

WHO Global Model Regulatory Framework for Medical Devices including IVD medical devices

This document was adopted by the WHO Expert Committee on Specifications for Pharmaceutical Preparations at its 51st meeting, which took place in Geneva from 17 to 21 October 2016, and will be published as Annex 4 to its report: Fifty-first report of the WHO Expert Committee on specifications for pharmaceutical preparations (WHO technical report series; no. 1003).

2017 Jan

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File Type: pdf
Category: Other documents, WHO document
Unit: Medical Devices