- Application of the rapid ethical assessment approach to enhance the ethical conduct of longitudinal population based female cancer research in an urban setting in Ethiopia
- Challenges arising when seeking broad consent for health research data sharing: a qualitative study of perspectives in Thailand
- Impact of moral case deliberation in healthcare settings: a literature review
- Addressing vaccine hesitancy requires an ethically consistent health strategy
- Ethical considerations for HIV cure-related research at the end of life
- Conscientious objection to intentional killing: an argument for toleration
- Exploring neurologists’ perspectives on the return of next generation sequencing results to their patients: a needed step in the development of guidelines
- Attitudes to prenatal screening among Norwegian citizens: liberality, ambivalence and sensitivity
- What information and the extent of information research participants need in informed consent forms: a multi-country survey
- A bioethical framework to guide the decision-making process in the care of seriously ill patients
- Reuse of cardiac organs in transplantation: an ethical analysis
- Frequency of use of the religious exemption in New Jersey cases of determination of brain death
- The values and ethical commitments of doctors engaging in macroallocation: a qualitative and evaluative analysis
- Beyond ‘health and safety’ – the challenges facing students asked to work outside of their comfort, qualification level or expertise on medical elective placement
- A systematic review of the literature on ethical aspects of transitional care between child- and adult-orientated health services
- Setting standards for empirical bioethics research: a response to Carter and Cribb
- Debating diversity: a commentary on Standards of practice in empirical bioethics research
- Predictors of consent to cell line creation and immortalisation in a South African schizophrenia genomics study
- Let’s talk about standards: a commentary on standards of practice in empirical bioethics
- Standards of practice in empirical bioethics research: towards a consensus
- Their view: difficulties and challenges of patients and physicians in cross-cultural encounters and a medical ethics perspective
- Ethics of task shifting in the health workforce: exploring the role of community health workers in HIV service delivery in low- and middle-income countries
- Management of financial conflicts of interests in clinical practice guidelines in Germany: results from the public database GuidelineWatch
- Good health checks according to the general public; expectations and criteria: a focus group study
- Ethical challenges assessed in the clinical ethics Committee of Psychiatry in the region of Southern Denmark in 2010–2015: a qualitative content analyses
- Ethical competence in DNR decisions –a qualitative study of Swedish physicians and nurses working in hematology and oncology care
- Ethical concerns on sharing genomic data including patients’ family members
- A reflection on the challenge of protecting confidentiality of participants while disseminating research results locally
- Introduction to Ethics and Global Health
- Commodification of care and its effects on maternal health in the Noun division (West Region – Cameroon)
- Integrated primary health care in low- and middle-income countries: a double challenge
- In pursuit of goodness in bioethics: analysis of an exemplary article
- Evaluation as institution: a contractarian argument for needs-based economic evaluation
- Advance directive: does the GP know and address what the patient wants? Advance directive in primary care
- Opening the debate on deep brain stimulation for Alzheimer disease – a critical evaluation of rationale, shortcomings, and ethical justification
- Identification of ethics committees based on authors’ disclosures: cross-sectional study of articles published in the European Journal of Anaesthesiology and a survey of ethics committees
- The patient perspective in health care networks
- The significance of ethics reflection groups in mental health care: a focus group study among health care professionals
- Medicine, market and communication: ethical considerations in regard to persuasive communication in direct-to-consumer genetic testing services
- The dual use of research ethics committees: why professional self-governance falls short in preserving biosecurity
- Leadership in palliative medicine: moral, ethical and educational
- Changes in attitudes towards hastened death among Finnish physicians over the past sixteen years
- Surgical informed consent in obstetric and gynecologic surgeries: experience from a comprehensive teaching hospital in Southern Ethiopia
- Research ethics review at University Eduardo Mondlane (UEM)/Maputo Central Hospital, Mozambique (2013–2016): a descriptive analysis of the start-up of a new research ethics committee (REC)
- A scoping review of reporting ‘Ethical Research Practices’ in research conducted among refugees and war-affected populations in the Arab world
- Translating and culturally adapting the shortened version of the Hospital Ethical Climate Survey (HECS-S) – retaining or modifying validated instruments
- Involvement in decisions about intravenous treatment for nursing home patients: nursing homes versus hospital wards
- Complexity of consenting for medical termination of pregnancy: prospective and longitudinal study in Paris
- The involvement of Canadian physicians in promoting and providing unproven and unapproved stem cell interventions
- Conscientious objection to participation in abortion by midwives and nurses: a systematic review of reasons
- ‘Screening audit’ as a quality assurance tool in good clinical practice compliant research environments
- Patenting human genes: Chinese academic articles’ portrayal of gene patents
- Rationing elective surgery for smokers and obese patients: responsibility or prognosis?
- Women’s perspectives on the ethical implications of non-invasive prenatal testing: a qualitative analysis to inform health policy decisions
- Skepticism towards the Swedish vision zero for suicide: interviews with 12 psychiatrists
- Forensic psychiatry, one subspecialty with two ethics? A systematic review
- Ethical principles and placebo-controlled trials – interpretation and implementation of the Declaration of Helsinki’s placebo paragraph in medical research
- Compassionate use programs in Italy: ethical guidelines
- Educational video-assisted versus conventional informed consent for trauma-related debridement surgery: a parallel group randomized controlled trial
- Patient data and patient rights: Swiss healthcare stakeholders’ ethical awareness regarding large patient data sets – a qualitative study
- Early-career researchers’ views on ethical dimensions of patient engagement in research
- Leaving patients to their own devices? Smart technology, safety and therapeutic relationships
- The ethics of using placebo in randomised controlled trials: a case study of a Plasmodium vivax antirelapse trial
- Euthanasia and assisted suicide for people with an intellectual disability and/or autism spectrum disorder: an examination of nine relevant euthanasia cases in the Netherlands (2012–2016)
- Objectivity applied to embodied subjects in health care and social security medicine: definition of a comprehensive concept of cognitive objectivity and criteria for its application
- Screening for infectious diseases of asylum seekers upon arrival: the necessity of the moral principle of reciprocity
- Rules of engagement: perspectives on stakeholder engagement for genomic biobanking research in South Africa
- Matters to address prior to introducing new life support technology in Japan: three serious ethical concerns related to the use of left ventricular assist devices as destination therapy and suggested policies to deal with them
- Ethical issues in pragmatic randomized controlled trials: a review of the recent literature identifies gaps in ethical argumentation
- Ethical implications of digital communication for the patient-clinician relationship: analysis of interviews with clinicians and young adults with long term conditions (the LYNC study)
- Moral dilemmas and conflicts concerning patients in a vegetative state/unresponsive wakefulness syndrome: shared or non-shared decision making? A qualitative study of the professional perspective in two moral case deliberations
- Advance directives as a tool to respect patients’ values and preferences: discussion on the case of Alzheimer’s disease
- Disparate compensation policies for research related injury in an era of multinational trials: a case study of Brazil, Russia, India, China and South Africa
- Benefit in liver transplantation: a survey among medical staff, patients, medical students and non-medical university staff and students
- An update on the “empirical turn” in bioethics: analysis of empirical research in nine bioethics journals
- Combining value of information analysis and ethical argumentation in decisions on participation of vulnerable patients in clinical research
- Fake facts and alternative truths in medical research
- Autonomy and couples’ joint decision-making in healthcare
- “Right to recommend, wrong to require”- an empirical and philosophical study of the views among physicians and the general public on smoking cessation as a condition for surgery
- Ethical aspects of diagnosis and interventions for children with fetal alcohol Spectrum disorder (FASD) and their families
- Balancing the local and the universal in maintaining ethical access to a genomics biobank
- The use of empirical research in bioethics: a survey of researchers in twelve European countries
- Participatory improvement of a template for informed consent documents in biobank research – study results and methodological reflections
- Ethical challenges experienced by UK military medical personnel deployed to Sierra Leone (operation GRITROCK) during the 2014–2015 Ebola outbreak: a qualitative study
- Experiences of community members and researchers on community engagement in an Ecohealth project in South Africa and Zimbabwe
- The ethics of caring for hospital-dependent patients
- Decision-making on therapeutic futility in Mexican adolescents with cancer: a qualitative study
- Transplant eligibility for patients with affective and psychotic disorders: a review of practices and a call for justice
- Must we remain blind to undergraduate medical ethics education in Africa? A cross-sectional study of Nigerian medical students
- Attitudes towards assisted suicide and euthanasia among care-dependent older adults (50+) in Austria: the role of socio-demographics, religiosity, physical illness, psychological distress, and social isolation
- Patient-targeted Googling and social media: a cross-sectional study of senior medical students
- Informed consent for clinical treatment in low-income setting: evaluating the relationship between satisfying consent and extent of recall of consent information
- Roles and responsibilities of clinical ethics committees in priority setting
- Ethical considerations in forensic genetics research on tissue samples collected post-mortem in Cape Town, South Africa
- Development and pilot testing of an informed consent video for patients with limb trauma prior to debridement surgery using a modified Delphi technique
- Measuring inconsistency in research ethics committee review
- The no correlation argument: can the morality of conscientious objection be empirically supported? the Italian case
- Biobanking in Israel 2016–17; expressed perceptions versus real life enrollment
- Gender and age disparity in the initiation of life-supporting treatments: a population-based cohort study
- The strange case of Mr. H. Starting dialysis at 90 years of age: clinical choices impact on ethical decisions
- Ethical aspects of brain computer interfaces: a scoping review
- The emergence of ethical issues in the provision of online sexual health outreach for gay, bisexual, two-spirit and other men who have sex with men: perspectives of online outreach workers
- This moral coil: a cross-sectional survey of Canadian medical student attitudes toward medical assistance in dying
- Collaborative partnership and the social value of clinical research: a qualitative secondary analysis
- Limits to human enhancement: nature, disease, therapy or betterment?
- What is a good health check? An interview study of health check providers’ views and practices
- Descriptive study of association between quality of care and empathy and burnout in primary care
- Informed consent and registry-based research – the case of the Danish circumcision registry
- Erratum to: The Liverpool Care Pathway: discarded in cancer patients but good enough for dying nursing home patients? A systematic review
- Eliciting meta consent for future secondary research use of health data using a smartphone application – a proof of concept study in the Danish population
- Ethical issues of informed consent in malaria research proposals submitted to a research ethics committee in Thailand: a retrospective document review
- Does growing up with a physician influence the ethics of medical students’ relationships with the pharmaceutical industry? The cases of the US and Poland
- The Liverpool Care Pathway: a systematic review discarded in cancer patients but good enough for dying nursing home patients?
- Healthcare professionals’ and patients’ perspectives on consent to clinical genetic testing: moving towards a more relational approach
- Pre- and post-testing counseling considerations for the provision of expanded carrier screening: exploration of European geneticists’ views
- Erratum to: Ethics review of studies during public health emergencies – the experience of the WHO ethics review committee during the Ebola virus disease epidemic
- Familiar ethical issues amplified: how members of research ethics committees describe ethical distinctions between disaster and non-disaster research
- Ethics review of studies during public health emergencies – the experience of the WHO ethics review committee during the Ebola virus disease epidemic
- Comparative effectiveness research: what to do when experts disagree about risks
- Development of a consensus operational definition of child assent for research
- Are advance directives helpful for good end of life decision making: a cross sectional survey of health professionals
- How Chinese clinicians face ethical and social challenges in fecal microbiota transplantation: a questionnaire study
- A 14-day limit for bioethics: the debate over human embryo research
- Staff’s normative attitudes towards coercion: the role of moral doubt and professional context—a cross-sectional survey study
- Written versus verbal consent: a qualitative study of stakeholder views of consent procedures used at the time of recruitment into a peripartum trial conducted in an emergency setting
- A qualitative study on acceptable levels of risk for pregnant women in clinical research
- The Picture Talk Project: Starting a Conversation with Community Leaders on Research with Remote Aboriginal Communities of Australia
- Self-tests for influenza: an empirical ethics investigation
- Assessment of knowledge about biobanking among healthcare students and their willingness to donate biospecimens
- On classifying the field of medical ethics
- Ethics of health research with prisoners in Canada
- Core information sets for informed consent to surgical interventions: baseline information of importance to patients and clinicians
- The elusive ideal of inclusiveness: lessons from a worldwide survey of neurologists on the ethical issues raised by whole-genome sequencing
- A critique of the regulation of data science in healthcare research in the European Union
- Fair is fair: We must re-allocate livers for transplant
- Smart homes, private homes? An empirical study of technology researchers’ perceptions of ethical issues in developing smart-home health technologies
- Factors affecting willingness to share electronic health data among California consumers