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“…Overall, I argue that genomic data, by virtue of their distributed and shared nature, necessitate novel approaches for bioethical assessment.…”
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“…It also led to a creative long-term research partnership, initiated a long-term programme of public education in the UK about reproductive science and stimulated the development of bioethical thinking.…”
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“…Reviewing the publications of prominent American rabbis who have (extensively) published on Jewish biomedical ethics, this article highlights Orthodox, Conservative and Reform opinions on a most pressing contemporary bioethical issue: euthanasia. Reviewing their opinions against the background of the halachic character of Jewish (biomedical) ethics, this article shows how from one traditional Jewish textual source diverse, even contradictory, opinions emerge through different interpretations. …”
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“…An ethical framework for the acceptability of such experiments is developed based on the bioethical principles for experiments with human subjects: non-maleficence, beneficence, respect for autonomy, and justice. …”
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“…Among those, we discuss here the bioethical implications of preserving individual freedom in the context of the early response to a pandemic and propose a global approach to the issue that could be applied in future health challenges.…”
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“…The report was structured around the four bioethical principles. RESULTS: health care for trans people is complex, transversal to many devices and specialties and longitudinal in time, that is why it requires coordinated action. …”
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“…In the last 50 years researches in the field of allotransplantation led to obtaining promising results for solving difficult cases when autologous tissues are not available for reconstruction, despite all the bioethical issues of this subject. This field of composite tissue transplantation evolved constantly, the top of it being total face transplantation, successfully accomplished while being based on the knowledge accumulated. …”
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“…However there is an ongoing discussion in bioethical circles on the level of comprehension of the informed consent process by the patients and research participants. …”
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