CorrespondenceData protection and consent to biomedical research: a step forward?
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Observational health research in Europe: understanding the General Data Protection Regulation and underlying debate
2018, European Journal of CancerCitation Excerpt :Regarding research, the European Parliament (EP) took that to the extreme with a ‘consent or anonymise’ approach in its 2014 version of the draft GDPR [2] in spite of existing criticism in the literature about that approach [3]. Worried comments from researchers and patient organisations followed [2,4–7]. The Wellcome Trust with the website datasaveslives (now with a different content) [8] has been extremely helpful in bundling efforts.
Comparable indicators of therapeutic misconception between epilepsy or Parkinson's disease patients between those with clinical trial experience and trial non-participants
2018, SeizureCitation Excerpt :As for future trials, three quarters of our CT participant subjects concluded that new consent should be sought if the CT data were to be used for other research purposes. This issue has been given attention globally and remains under debate [32,33]. Our study has some limitations.
A step forward for data protection and biomedical research
2016, The LancetData donation after death
2015, The LancetMedical Information Commons: Conceptual, Legal and Ethical Considerations for Stakeholders
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