Information required together with your MDR application (appendix A, B, C) – best practices

The Medical Device Regulation (MDR) 2017/745 updates the legal framework for all medical devices intended to be placed on the European market.   

In this hands-on session, you learn which information is required together with the application for an MDR conformity assessment with TÜV SÜD Product Service GmbH. We will focus on the application appendix A, B and C and the list of CE-marked devices, which are the data basis for the complete conformity assessment procedure and the resulting certification cycle. Best-practice examples will be presented and discussed, allowing enough time for your questions. The on-time submission of the complete set of required information guarantees the proper and goal-oriented processing of your application.

Date and time: Monday, 24 October 2022, 1:00 pm (CEST​​​​​​​/ 7.00 am (EDT)

Your speakers: Annika Fröhlich, Product Specialist & Auditor


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