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