Hands-on session*: MDR application forms

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

This hands-on session shall provide guidance on how to fill out the required MDR application form and applicable appendices for an MDR conformity assessment with TÜV SÜD Product Service GmbH. A special focus will be laid on the most common pitfalls that can be avoided to speed up your application process. Providing the complete information in time guarantees a proper and goal-oriented processing of your application. 

Date and time: Tuesday, 9 November 2021, 10.00 am (CET)

Your speakers: Annika Fröhlich | Global Process Owner Application Management
                             Christian Schröder | Deputy Global Process Owner Application Management

*Only for existing customers

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