Governance, Innovation and AI-Powered solutions in the global regulation of MedTech

Available on-demand

Webinar

The MedTech regulatory industry is notoriously complex, due to a combination of factors such as diverse global standards, evolving technologies and varying risk classifications.

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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Meet the Speakers

Mike King

Senior Director of Product and Strategy at IQVIA

Roy Zhu

Regulatory Affairs and Quality Assurance Director, APAC RCO Quality & Regulatory at Dentsply Sirona

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