Article metrics
PDF
Other content recommended for you
- The perils of a broad approach to public interest in health data research: a response to Ballantyne and Schaefer
- Consent and the ethical duty to participate in health data research
- Taxonomy of justifications for consent waivers: When and why are public views relevant?
- Research or clinical care: what’s the difference?
- Genetic research and the collective good: participants as leaders to reconcile individual and public interests
- Patient data for commercial companies? An ethical framework for sharing patients’ data with for-profit companies for research
- Machine learning models, trusted research environments and UK health data: ensuring a safe and beneficial future for AI development in healthcare
- Patients’ and public views and attitudes towards the sharing of health data for research: a narrative review of the empirical evidence
- Multiple modes of data sharing can facilitate secondary use of sensitive health data for research
- Challenges to biobanking in LMICs during COVID-19: time to reconceptualise research ethics guidance for pandemics and public health emergencies?