Patient data and patient rights: Swiss healthcare stakeholders’ ethical awareness regarding large patient data sets – a qualitative study

Abstract 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 insti...

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Bibliographic Details
Main Authors: Corine Mouton Dorey, Holger Baumann, Nikola Biller-Andorno
Format: Article
Language:English
Published: BMC 2018-03-01
Series:BMC Medical Ethics
Subjects:
Online Access:http://link.springer.com/article/10.1186/s12910-018-0261-x