Informed consent and registry-based research – the case of the Danish circumcision registry

BMC Medical Ethics 2017 18:53
Authors: Thomas Ploug, Søren Holm
“Research into personal health data holds great potential not only for improved treatment but also for economic growth. In these years many countries are developing policies aimed at facilitating such research often under the banner of ‘big data’. A central point of debate is whether the secondary use of health data requires informed consent if the data is anonymised.”
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