Global In Vitro Diagnostics (IVD) and Medical Device Regulatory Modernization Efforts

This lecture examines global regulatory modernization efforts over the past decade that have significantly impacted medical devices and in vitro diagnostic (IVD) devices internationally. The session will explore the driving forces behind these regulatory changes and provide a status update, evaluating what has succeeded, what has encountered challenges, and what developments may emerge next.
Learning Objectives:
Attendees will

Learn about recent key changes in medical device and IVD regulations globally
Gain understanding of implementation successes and challenges
Explore emerging regulatory modernization efforts and future trends

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