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The top documents tagged [broad consent]
Biobanks, data protection and issues of integrity Finnish and Nordic perspectives
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What Should You Know and Be Doing About Genome Privacy? Ellen Wright Clayton, MD, JD Center for Biomedical Ethics and Society Vanderbilt University
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Making Qualitative Data Open - Libby Bishop, UK Data Service
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Bishop open qual_recode_sheffield_14_15may2015 (3)
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Protecting Participants in a Global Research Community Dr. Jane Kaye University of Oxford, UK
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Relations matter: A solidarity-based perspective on data-rich medicine TRANSLATION IN HEALTHCARE- EXPLORING THE IMPACT OF EMERGING TECHNOLOGIES University
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CERC/CERC SURVEY WORK GROUP Presented by: Maureen Smith and Ingrid Holm For the CERC Survey Work Group eMERGE Steering Committee Meeting June 29-30, 2015
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Electronic Medical Records and Genomics ( eMERGE ) Network Phase III
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