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Patient data and patient rights: Swiss healthcare stakeholders’ ethical awareness regarding large patient data sets – a qualitative study
BACKGROUND: There is a growing interest in aggregating more biomedical and patient data into large health data sets for research and public benefits. However, collecting and processing patient data raises new ethical issues regarding patient’s rights, social justice and trust in public institutions....
Autores principales: | Mouton Dorey, Corine, Baumann, Holger, Biller-Andorno, Nikola |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5842517/ https://www.ncbi.nlm.nih.gov/pubmed/29514635 http://dx.doi.org/10.1186/s12910-018-0261-x |
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