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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 TÃœV SÃœD 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