This on-demand webinar, hosted by Greenlight Guru, delves into the nuances of the medical device classification system. It explores how to use the classification system to gain a competitive advantage and efficiently navigate regulatory pathways.

Watch this session to gain insights into the complexities and strategic aspects of device classification.

Main points covered:
1. Overview of the medical device classification system.
2. Importance and impact of the classification system.
3. Strategies for determining and potentially changing device classification.
4. Influence of labeling and risk on classification.
5. Global variations in device classification and recent updates.

Target Audience:
• Medical Device Executives
• Regulatory Affairs Professionals and Management
• Quality Professionals and Management
• Clinical Affairs Professionals and Management
• R&D Engineers and Management

Access the printable slides for this presentation by visiting:
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