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2.
Trends Biotechnol ; 38(4): 351-354, 2020 04.
Article in English | MEDLINE | ID: mdl-32014274

ABSTRACT

As public interest advocates, policy experts, bioethicists, and scientists, we call for a course correction in public discussions about heritable human genome editing. Clarifying misrepresentations, centering societal consequences and concerns, and fostering public empowerment will support robust, global public engagement and meaningful deliberation about altering the genes of future generations.


Subject(s)
Gene Editing/ethics , Genome, Human/genetics , Bioethical Issues , Embryo, Mammalian , Germ Cells , Humans
6.
J Law Biosci ; 4(1): 175-180, 2017 Apr.
Article in English | MEDLINE | ID: mdl-28852562
7.
BMC Med Ethics ; 17(1): 74, 2016 11 14.
Article in English | MEDLINE | ID: mdl-27842524

ABSTRACT

New technologies are transforming and reconfiguring the boundaries between patients, research participants and consumers, between research and clinical practice, and between public and private domains. From personalised medicine to big data and social media, these platforms facilitate new kinds of interactions, challenge longstanding understandings of privacy and consent, and raise fundamental questions about how the translational patient pathway should be organised.This editorial introduces the cross-journal article collection "Translation in healthcare: ethical, legal, and social implications", briefly outlining the genesis of the collection in the 2015 Translation in healthcare conference in Oxford, UK and providing an introduction to the contemporary ethical challenges of translational research in biology and medicine accompanied by a summary of the papers included in this collection.


Subject(s)
Bioethical Issues , Delivery of Health Care/ethics , Translational Research, Biomedical/ethics , Community Participation , Confidentiality , Delivery of Health Care/legislation & jurisprudence , Ethics, Clinical , Humans , Informed Consent , Precision Medicine , Privacy , Research Subjects , Social Media , Translational Research, Biomedical/legislation & jurisprudence
8.
CMAJ ; 2016 Mar 21.
Article in English | MEDLINE | ID: mdl-27001740
9.
New Bioeth ; 19(1): 18-29, 2013.
Article in English | MEDLINE | ID: mdl-24707594

ABSTRACT

After the development of induced pluripotent stem cells (IPSCs) in 2007, the pressure to commercialize women's eggs for stem cell research could have been expected to lessen. However, the pressure to harvest human eggs in large quantities for research has not diminished; rather, it has taken different directions, for example in germline mitochondrial research. Yet there has been little acknowledgement of these technologies' need for human eggs, the possible risks to women and the ethical issues concerning potential exploitation. Rather, there has been a renewed campaign to legalize payment for eggs in research, although the actual scientific advances are at best modest. This article shows why a market in women's eggs is ethically problematic in terms of the doctor's duty to do no harm and the limitations of 'informed' consent.


Subject(s)
Commodification , Embryo Research/ethics , Informed Consent , Mitochondria , Nuclear Transfer Techniques/ethics , Ovum , Reimbursement Mechanisms , Tissue Donors , Female , Humans , Korea , Mitochondria/transplantation , Nuclear Transfer Techniques/trends , Stem Cells , United States
10.
Indian J Med Ethics ; 8(3): 175-9, 2011.
Article in English | MEDLINE | ID: mdl-22106647

ABSTRACT

Whilst India has been debating how to regulate 'surrogacy' the UK has undergone a major consultation on increasing the amount of 'expenses'paid to egg 'donors', while France has recently finished debating its entire package of bioethics regulation and the role of its Biomedicine Agency. Although it is often claimed that there is no alternative to the neo-liberal, market-based approach in regulating (or not) reproductive medicine--the ideology prevalent in both India and the UK--advocates of that position ignore the alternative model offered by France's tighter regulation, as well as its overarching concern with protecting the vulnerable and ensuring social justice. Whilst the concepts underpinning the French model of regulation also have their provenance in Western political philosophy and not in the developed world, they embody a very different attitude and suggest that there is indeed an alternative to letting the market decide. However, even in France that alternative is highly contested.


Subject(s)
Public Policy , Remuneration , Reproductive Techniques, Assisted/economics , Reproductive Techniques, Assisted/legislation & jurisprudence , Social Control, Formal/methods , Tissue and Organ Procurement/economics , Tissue and Organ Procurement/legislation & jurisprudence , France , Humans , Ovum , Reproductive Techniques, Assisted/ethics , Tissue Donors/ethics , Tissue Donors/legislation & jurisprudence , Tissue and Organ Procurement/ethics , United Kingdom
12.
Bioethics ; 20(3): 115-24, 2006 Jun.
Article in English | MEDLINE | ID: mdl-17039630

ABSTRACT

Prominent international and national ethics commissions such as the UNESCO International Bioethics Committee rarely achieve anything remotely resembling gender equality, although local research and ethics committees are somewhat more egalitarian. Under-representation of women is particularly troubling when the subject matter of modern bioethics so disproportionately concerns women's bodies, and when such committees claim to derive 'universal' standards. Are women missing from many ethics committees because of relatively straightforward, if discriminatory, demographic factors? Or are the methods of analysis and styles of ethics to which these bodies are committed somehow 'anti-female'? It has been argued, for example, that there is a 'different voice' in ethical reasoning, not confined to women but more representative of female experience. Similarly, some feminist writers, such as Evelyn Fox Keller and Donna Haraway, have asked difficult epistemological questions about the dominant 'masculine paradigm' in science. Perhaps the dominant paradigm in ethics committee deliberation is similarly gendered? This article provides a preliminary survey of women's representation on ethics committees in eastern and western Europe, a critical analysis of the supposed 'masculinism' of the principlist approach, and a case example in which a 'different voice' did indeed make a difference.


Subject(s)
Advisory Committees/organization & administration , Committee Membership , Ethics Committees/organization & administration , Women , Bioethics , Data Collection , Empathy , Europe , Female , Feminism , Hand Transplantation , Humans , Internationality , Male , Medicine , Personal Autonomy , Personality Development , Principle-Based Ethics , Science , Sex Factors
14.
Dev World Bioeth ; 4(2): 109-24, 2004 Dec.
Article in English | MEDLINE | ID: mdl-15516211

ABSTRACT

The global value of the biotechnology industry is now estimated at 17 billion dollars, with over 1300 firms involved as of the year 2000.(2) It has been said that 'What we are witnessing is nothing less than a new kind of gold rush, and the territory is the body.' As in previous gold rushes, prospectors are flooding into unexplored and 'wide open' territories from all over the world, with possible ramifications for exploitation of Third World populations. These territories are also the Wild West of bioethics insofar as the law has very little hold on them: existing medical and patent law, such as the Moore and Chakrabarty cases, exert little control over powerful economic interests in both the United States and Europe. In the absence of a unified and consistent law on property in the body, the focus is increasingly on refining the consent approach to rights in human tissue and the human genome, with sensitive and promising developments from the Human Genetics Commission and the Department for International Development consultation on intellectual property. These developments incorporate the views of vulnerable genetic communities such as Native Americans or some Third World populations, and should be welcomed because they recognise the power imbalance between such groups and First World researchers or firms. However, they also highlight the continued tension about what is really wrong with commodifying human tissue or the human genome. Where's the injustice, and can it be solved by a more sophisticated consent procedure?


Subject(s)
Commodification , Developing Countries , Ethnicity/genetics , Genetic Research/ethics , Human Body , Informed Consent/ethics , Vulnerable Populations , Coercion , Developed Countries , Humans , Ownership , Patents as Topic/ethics , Research Subjects/economics , Social Justice , Tissue Donors
19.
Dev World Bioeth ; 2(1): 55-63, 2002 May.
Article in English | MEDLINE | ID: mdl-12872770

ABSTRACT

One effect of late capitalism--the commodification of practically everything--is to knock down the Chinese walls between the natural and productive realms, to use a Marxist framework. Women's labour in egg extraction and 'surrogate' motherhood might then be seen as what it is, labour which produces something of value. But this does not necessarily mean that women will benefit from the commodification of practically everything, in either North or South. In the newly developing biotechnologies involving stem cells, the reverse is more likely, particular given the the shortage in the North of the egg donors who will be increasingly necessary to therapeutic cloning. Although most of the ethical debate has focused on the status of the embryo, this is to define ethics with no reference to global or gender justice. There has been little or no debate about possible exploitation of women, particularly of ovum donors from the South. Countries of the South without national ethics committees or guidelines may be particularly vulnerable: although there is increasing awareness of the susceptibility of poorer countries to abuses in research ethics, very little has been written about how they might be affected by the enormously profitable new technologies exploiting human tissue. Even in the UK, although the new Medical Research Council guidelines make a good deal of the 'gift relationship', what they are actually about is commodification. If donors believe they are demonstrating altruism, but biotechnology firms and researchers use the discourse of commodity and profit, we have not 'incomplete commodification' but complete commodification with a plausibly human face.


Subject(s)
Commodification , Feminism , Ownership , Stem Cells , Tissue Donors , Women , Biotechnology/ethics , Capitalism , Cloning, Organism , Developing Countries , Embryo Research , Embryo, Mammalian , Europe , Female , Germ Cells , Humans , Internationality , Oocyte Donation , Ownership/legislation & jurisprudence , United States , Women's Rights
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