placing innovative medical devices on market

Navigating the EU market to place innovative devices




Meeting the requirements for innovative medical devices has become more challenging ever since MDR and IVDR were enforced. This has led to discussions within the EU commission in Brussels aiming to improve the legislation in the future. This session will give a comprehensive overview of this discussion and potential changes. Furthermore, it will provide manufacturers with comprehensive knowledge on how to best navigate the EU market and successfully launch their innovations until any changes might be enforced. 

About the speakers

Digital DialoguesDr Royth von Hahn | Dr Sabina Hoekstra

Senior Vice President, TÜV SÜD MHS | Global Director Regulatory Strategy, TÜV SÜD MHS






Note: The video was recorded in October 2023 – no liability for any changes.

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