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Editions published in BMC Medical Ethics 200
Too many entities requested (1011). Only 200 are displayed.
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Self-tests for influenza: an empirical ethics investigation
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The Picture Talk Project: Starting a Conversation with Community Leaders on Research with Remote Aboriginal Communities of Australia
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Core information sets for informed consent to surgical interventions: baseline information of importance to patients and clinicians.
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The ECOUTER methodology for stakeholder engagement in translational research.
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Smart homes, private homes? An empirical study of technology researchers' perceptions of ethical issues in developing smart-home health technologies
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Familiar ethical issues amplified: how members of research ethics committees describe ethical distinctions between disaster and non-disaster research
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The elusive ideal of inclusiveness: lessons from a worldwide survey of neurologists on the ethical issues raised by whole-genome sequencing
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Ethics of health research with prisoners in Canada
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Assessment of knowledge about biobanking among healthcare students and their willingness to donate biospecimens
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A qualitative study on acceptable levels of risk for pregnant women in clinical research
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Citizen science or scientific citizenship? Disentangling the uses of public engagement rhetoric in national research initiatives
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Has the biobank bubble burst? Withstanding the challenges for sustainable biobanking in the digital era
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If you build it, they will come: unintended future uses of organised health data collections
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Perceptions of the general public and physicians regarding open disclosure in Korea: a qualitative study
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Dying well with reduced agency: a scoping review and thematic synthesis of the decision-making process in dementia, traumatic brain injury and frailty
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What do international ethics guidelines say in terms of the scope of medical research ethics?
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Introduction to the article collection 'Translation in healthcare: ethical, legal, and social implications'
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Public responses to the sharing and linkage of health data for research purposes: a systematic review and thematic synthesis of qualitative studies
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Young people's views about the purpose and composition of research ethics committees: findings from the PEARL qualitative study
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National ethics guidance in Sub-Saharan Africa on the collection and use of human biological specimens: a systematic review
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Between Scylla and Charybdis: reconciling competing data management demands in the life sciences
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Qualitative study on custodianship of human biological material and data stored in biobanks
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Ethical issues in using Twitter for population-level depression monitoring: a qualitative study
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The badness of death and priorities in health.
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HIV/AIDS clients, privacy and confidentiality; the case of two health centres in the Ashanti Region of Ghana
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"It's all about trust": reflections of researchers on the complexity and controversy surrounding biobanking in South Africa
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Seeking consent for research with indigenous communities: a systematic review
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Next of kin's experiences of involvement during involuntary hospitalisation and coercion
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23andMe: a new two-sided data-banking market model
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The importance of values in evidence-based medicine
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Research participants' perceptions and views on consent for biobank research: a review of empirical data and ethical analysis
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Co-design and implementation research: challenges and solutions for ethics committees
Subject - wd:Q15762173