Webinar
Webinar
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.
Dr 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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