Guidance on the renewal of designation and monitoring of notified bodies under Directives 90/385/EEC and 93/42/EEC to be performed in accordance with Commission Implementing Regulation (EU) 2020/666 amending Commission Implementing Regulation (EU) 920/2013
Information
Type
Guidance
Regulated products
Medical Devices
Topics
Notified Bodies
Published
May 1, 2020
Last updated
May 1, 2020
Description
This document provides guidance on the renewal and monitoring of notified bodies under EU Directives 90/385/EEC and 93/42/EEC.
Tags
Organization
Country / Region
European Union
License
Creative Commons Attribution 4.0