Share
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?
- Patients’ and public views and attitudes towards the sharing of health data for research: a narrative review of the empirical evidence
- Challenges to biobanking in LMICs during COVID-19: time to reconceptualise research ethics guidance for pandemics and public health emergencies?
- 'It’s not something you can take in your hands'. Swiss experts’ perspectives on health data ownership: an interview-based study
- Legal and ethical considerations in processing patient-identifiable data without patient consent: lessons learnt from developing a disease register
- How should we think about clinical data ownership?
- Legal aspects of records based medical research