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Governance, Innovation and AI-Powered solutions in the Global Regulation of MedTech

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In this webinar, IQVIA explores the intricate landscape of medical devices and technologies, and the complex regulatory environment that governs the industry on a global scale.


In this webinar, you will learn:


  • How the role of eQMS and end-to-end workflows are essential in facilitating compliance, efficiency and strategic positioning of devices and technologies
  • Why understanding the regulatory landscape, classification of devices and adherence to QMS standards, is vital for regulatory approval and market access in China
  • The significance of local expertise when navigating the diverse regulatory landscape in the APAC


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