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

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

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