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The federal government has put a lot of resources behind the concept of patient-centered outcomes research. So with large clinical research projects, what would patient-centric research look like? And how are big data, mobile apps and new approaches to consent involved?

The federal government has put a lot of resources behind the concept of patient-centered outcomes research. So with large clinical research projects, what would patient-centric research look like? And how are big data, mobile apps and new approaches to consent involved?

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