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Human Factors & Risk Management: What's Needed & Why?

Global Medical Device Podcast powered by Greenlight Guru

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Product Development

If you're a URRA is not scoped appropriately your validation will never be completely comprehensive. Well, that to me says you need to bring that right up alongside product development. And they've got to be partners from the very beginning. It's an exciting tool, and just seeing people I love to I teach as well with pathway for patient health in the quality science curriculum. Seeing that done well and early in a project, it is so valuable.

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