BMC Medical Ethics

Does written informed consent adequately inform surgical patients? A cross sectional study

Euthanasia requests in dementia cases; what are experiences and needs of Dutch physicians? A qualitative interview study

Research approvals iceberg: how a ‘low-key’ study in England needed 89 professionals to approve it and how we can do better

Experiences from a community advisory Board in the Implementation of early access to ART for all in Eswatini: a qualitative study

Perceptions and intentions toward medical assistance in dying among Canadian medical students

Public and physicians’ support for euthanasia in people suffering from psychiatric disorders: a cross-sectional survey study

How to tackle the conundrum of quality appraisal in systematic reviews of normative literature/information? Analysing the problems of three possible strategies (translation of a German paper)

The challenge of community engagement and informed consent in rural Zambia: an example from a pilot study

Secularity, abortion, assisted dying and the future of conscientious objection: modelling the relationship between attitudes

Huge variation in obtaining ethical permission for a non-interventional observational study in Europe

Trust and the ethical challenges in the use of whole genome sequencing for tuberculosis surveillance: a qualitative study of stakeholder perspectives

Illness and disease: an empirical-ethical viewpoint

Methodological challenges in European ethics approvals for a genetic epidemiology study in critically ill patients: the GenOSept experience

Implementing ethics reflection groups in hospitals: an action research study evaluating barriers and promotors

Mapping, framing, shaping: a framework for empirical bioethics research projects

Informed consent and community engagement in open field research: lessons for gene drive science

The psychology of “cure” - unique challenges to consent processes in HIV cure research in South Africa

Clinical ethics dilemmas in a low-income setting - a national survey among physicians in Ethiopia

The involvement of family in the Dutch practice of euthanasia and physician assisted suicide: a systematic mixed studies review

Attitudes of Iranian students about organ donation: a qualitative study

The effects of industry funding and positive outcomes in the interpretation of clinical trial results: a randomized trial among Dutch psychiatrists

Ethical issues associated with HIV molecular epidemiology: a qualitative exploratory study using inductive analytic approaches

Nursing and midwifery students’ attitudes towards principles of medical ethics in Kermanshah, Iran

Lessons learned from implementing a responsive quality assessment of clinical ethics support

Truth-telling and doctor-assisted death as perceived by Israeli physicians

Vulnerability identified in clinical practice: a qualitative analysis

Influence of response shift and disposition on patient-reported outcomes may lead to suboptimal medical decisions: a medical ethics perspective

Legal medicine implications in fibrinolytic therapy of acute ischemic stroke

Ethical issues in denial of church wedding based on couple’s hemoglobin genotype in Enugu, south eastern Nigeria

Advance directives in France: do junior general practitioners want to improve their implementation and usage? A nationwide survey

Mention of ethical review and informed consent in the reports of research undertaken during the armed conflict in Darfur (2004–2012): a systematic review

Do codes of ethics and position statements help guide ethical decision making in Australian immigration detention centres?

Effect of written outcome information on attitude of perinatal healthcare professionals at the limit of viability: a randomized study

Ghent University Hospital’s protocol regarding the procedure concerning euthanasia and psychological suffering

A survey in Mexico about ethics dumping in clinical research

Experience of oncology residents with death: a qualitative study in Mexico

Can clinical ethics committees be legitimate actors in bedside rationing?

Engaging research ethics committees to develop an ethics and governance framework for best practices in genomic research and biobanking in Africa: the H3Africa model

Are physicians on the same page about do-not-resuscitate? To examine individual physicians’ influence on do-not-resuscitate decision-making: a retrospective and observational study

Infringement of the right to surgical informed consent: negligent disclosure and its impact on patient trust in surgeons at public general hospitals – the voice of the patient

What do patients with unmet medical needs want? A qualitative study of patients’ views and experiences with expanded access to unapproved, investigational treatments in the Netherlands

Reprogenetics, reproductive risks and cultural awareness: what may we learn from Israeli and Croatian medical students?

Dying too soon or living too long? Withdrawing treatment from patients with prolonged disorders of consciousness after Re Y

When patient advocacy organizations meet industry: a novel approach to dealing with financial conflicts of interest

Response to Correspondence from Kolstoe and colleagues concerning our paper entitled, Research approvals iceberg: How a ‘low-key’ study in England needed 89 professionals to approve it and how we can do better

Ethical tensions in the informed consent process for randomized clinical trials in emergency obstetric and newborn care in low and middle-income countries

Global health ethics: critical reflections on the contours of an emerging field, 1977–2015