RESUMO
Rapid release of prepublication data has served the field of genomics well. Attendees at a workshop in Toronto recommend extending the practice to other biological data sets.
Assuntos
Acesso à Informação , Guias como Assunto , Editoração , Pesquisa , Comportamento Cooperativo , Projeto Genoma Humano , Humanos , Ontário , Editoração/ética , Editoração/normas , Pesquisa/normas , Pesquisadores/ética , Pesquisadores/normasAssuntos
Privacidade Genética , Pesquisa em Genética/ética , Genômica , Acesso à Informação , Confidencialidade , Bases de Dados como Assunto , Genoma Humano , Health Insurance Portability and Accountability Act , Experimentação Humana/ética , Humanos , Disseminação de Informação , Consentimento Livre e Esclarecido , Estados UnidosRESUMO
In this fast-moving age of data banking, data are a currency, and often a commodity. Electronic health records are being developed everywhere. Increasingly, data collected for various primary purposes are being re-used for research. With personal mobility, contracting of services, and telemedicine, health care data are crossing national borders, and therefore so are genetic information, biological materials, and reimbursement data. There is much public and legal concern about the implications. This article addresses the question: Under what conditions may data not collected specifically for research, such as primary medical data, be re-used for health research without compromising the privacy of the data-subjects?
