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The Medical Device Innovation Consortium: joining public and private in the US to speed patient access to new technologies

This article was originally published in SRA

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Executive Summary

Dale Wahlstrom and Beth Lindborg explain how a new partnership between the US Food and Drug Administration and the private sector is working to validate tools and methods that will make the regulatory review process for medical devices more efficient.

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This copy is for your personal, non-commercial use. For high-quality copies or electronic reprints for distribution to colleagues or customers, please call +44 (0) 20 3377 3183

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