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1.
J Law Med Ethics ; 47(1): 12-20, 2019 03.
Article in English | MEDLINE | ID: mdl-30994067

ABSTRACT

Drawing on a landscape analysis of existing data-sharing initiatives, in-depth interviews with expert stakeholders, and public deliberations with community advisory panels across the U.S., we describe features of the evolving medical information commons (MIC). We identify participant-centricity and trustworthiness as the most important features of an MIC and discuss the implications for those seeking to create a sustainable, useful, and widely available collection of linked resources for research and other purposes.


Subject(s)
Community Participation , Information Dissemination , Medical Informatics/standards , Stakeholder Participation , Humans , Trust
2.
Trends Biotechnol ; 36(8): 741-743, 2018 08.
Article in English | MEDLINE | ID: mdl-29891181

ABSTRACT

A new infrastructure is urgently needed at the global level to facilitate exchange on key issues concerning genome editing. We advocate the establishment of a global observatory to serve as a center for international, interdisciplinary, and cosmopolitan reflection. This article is the second of a two-part series.


Subject(s)
Gene Editing/ethics , Gene Editing/methods , Capacity Building , Global Health , Humans
3.
Trends Biotechnol ; 36(7): 639-641, 2018 07.
Article in English | MEDLINE | ID: mdl-29871776

ABSTRACT

A new infrastructure is urgently needed at the global level to facilitate exchange on key issues concerning genome editing. We advocate the establishment of a global observatory to serve as a center for international, interdisciplinary, and cosmopolitan reflection. This article is the first of a two-part series.


Subject(s)
Bioethical Issues , Gene Editing/ethics , Gene Editing/legislation & jurisprudence , Humans
4.
Genome Med ; 9(1): 84, 2017 09 22.
Article in English | MEDLINE | ID: mdl-28938910

ABSTRACT

National and international public-private partnerships, consortia, and government initiatives are underway to collect and share genomic, personal, and healthcare data on a massive scale. Ideally, these efforts will contribute to the creation of a medical information commons (MIC), a comprehensive data resource that is widely available for both research and clinical uses. Stakeholder participation is essential in clarifying goals, deepening understanding of areas of complexity, and addressing long-standing policy concerns such as privacy and security and data ownership. This article describes eight core principles proposed by a diverse group of expert stakeholders to guide the formation of a successful, sustainable MIC. These principles promote formation of an ethically sound, inclusive, participant-centric MIC and provide a framework for advancing the policy response to data-sharing opportunities and challenges.


Subject(s)
Information Dissemination , Medical Informatics , Humans , Information Services , Medical Informatics/ethics
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