Alerts
PDF
Other content recommended for you
- Control, trust and the sharing of health information: the limits of trust
- Conditionally positive: a qualitative study of public perceptions about using health data for artificial intelligence research
- Multiple modes of data sharing can facilitate secondary use of sensitive health data for research
- Consent and the ethical duty to participate in health data research
- Big health data: the need to earn public trust
- Meta consent: a flexible and autonomous way of obtaining informed consent for secondary research
- In response to Ballantyne and Schaefer’s ‘Consent and the ethical duty to participate in health data research’
- Navigating data governance associated with real-world data for public benefit: an overview in the UK and future considerations
- Making consent for electronic health and social care data research fit for purpose in the 21st century
- Should free-text data in electronic medical records be shared for research? A citizens’ jury study in the UK