Why we should not seek individual informed consent for participation in health services research
Author:
Publisher
BMJ
Subject
Health Policy,Arts and Humanities (miscellaneous),Issues, ethics and legal aspects,Health(social science)
Cited by 56 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Structural under-reporting of informed consent, data handling and sharing, ethical approval, and application of Open Science principles as proxies for study quality conduct in COVID-19 research: a systematic scoping review;BMJ Global Health;2023-05
2. Is there a civic duty to support medical AI development by sharing electronic health records?;BMC Medical Ethics;2022-12-10
3. Building an Opt-Out Model for Service-Level Consent in the Context of New Data Regulations;Public Health Ethics;2022-01-11
4. Considerations for an integrated population health databank in Africa: lessons from global best practices;Wellcome Open Research;2021-08-23
5. Cluster randomised trials of prescribing policy: an ethical approach to generating drug safety evidence? A discussion of the ethical application of a new research method;Trials;2020-06-05
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