Abstract
A 2011 National Academies of Sciences report called for an “Information Commons” and a “Knowledge Network” to revolutionize biomedical research and clinical care. We interviewed 41 expert stakeholders to examine governance, access, data collection, and privacy in the context of a medical information commons. Stakeholders' attitudes about MICs align with the NAS vision of an Information Commons; however, differences of opinion regarding clinical use and access warrant further research to explore policy and technological solutions.
Original language | English (US) |
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Pages (from-to) | 41-50 |
Number of pages | 10 |
Journal | Journal of Law, Medicine and Ethics |
Volume | 47 |
Issue number | 1 |
DOIs |
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State | Published - Mar 1 2019 |
ASJC Scopus subject areas
- Medicine(all)