Children with medical complexities: their distinct vulnerability in health systems' Covid-19 response and their claims of justice in the recovery phase.
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Trust and the Goldacre Review: why trusted research environments are not about trust.
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A concentric circles view of health data relations facilitates understanding of sociotechnical challenges for learning health systems and the role of federated data networks.
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Changes in Healthcare Provision During Covid-19 and Their Impact on Children With Chronic Illness: A Scoping Review.
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Bans, Taxes or Product Placement? Applying the Liberal Perfectionist Proviso to Public Health Food Policy.
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Transformative disciplinary learning in history and social studies: Lessons from a high autonomy curriculum in New Zealand
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Wood BE. and Sheehan M., (2021), Curriculum Journal, 32, 495 - 509
Measuring the impact of participatory research in psychiatry: How the search for epistemic justifications obscures ethical considerations.
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Ethics review of big data research: What should stay and what should be reformed?
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Ethical Issues in Consent for the Reuse of Data in Health Data Platforms.
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The ethics of grandfather clauses in healthcare resource allocation.
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Development of a decision support intervention for family members of adults who lack capacity to consent to trials.
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'There's more to life than money and health': Family caregivers' views on the role of Power of Attorney in proxy decisions about research participation for people living with dementia.
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Decisions on Innovation or Research for Devastating Disease
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Public involvement in the governance of population-level biomedical research: unresolved questions and future directions.
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Tragic choices in intensive care during the COVID-19 pandemic: on fairness, consistency and community.
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Newdick C. et al, (2020), J Med Ethics, 46, 646 - 651
Constructing authentic decisions: proxy decision making for research involving adults who lack capacity to consent.
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Shepherd V. et al, (2020), J Med Ethics
'Your country needs you': the ethics of allocating staff to high-risk clinical roles in the management of patients with COVID-19.
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Dunn M. et al, (2020), J Med Ethics, 46, 436 - 440
Trust, trustworthiness and sharing patient data for research.
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Experimental Philosophical Bioethics.
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