eMDR Program and Process

If you don’t have a world-class Quality Management System, you may be falling behind. Your QMS can go beyond compliance as you work to enable a culture of True Quality. With QMS requirements changing, it’s important to understand how this will impact your business and product.

In this True Quality Summit Series, we’ll spend two days diving into the future of QMS requirements. Learn about upcoming deadlines, new changes, and what you can expect as you work towards a world-class QMS.

★ KEY VIDEO TAKEAWAY★

In this session we will learn about the Why, the What, the Who, and the How for Medical Device Reporting to FDA through eMDR Submissions.

This presentation originally aired during the 2022 Future of QMS Requirements Virtual Summit.

If you’d like to watch more related videos, browse through the full list of free replays from this track of the virtual summit event: https://www.youtube.com/playlist?list=PLkchw-at8PkMYKU4YINngG5ux9Gev72ps

Plus, download the slides for this presentation for free here: https://www.slideshare.net/greenlightguru/presentations

Are you looking for a MedTech Lifecycle Excellence (MLE) platform to help you bring safer medical devices to market faster with less risk? Take a quick tour of Greenlight Guru's MLE platform: https://www.greenlight.guru/medtech-lifecycle-excellence-platform

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Видео eMDR Program and Process канала Greenlight Guru