about
Citizen science or scientific citizenship? Disentangling the uses of public engagement rhetoric in national research initiativesPatient involvement in clinical research: why, when, and howKant, curves and medical learning practice: a reply to Le Morvan and Stock.The social licence for research: why care.data ran into trouble.The Ethics of Big Data: Current and Foreseeable Issues in Biomedical Contexts.Ethical Issues in Big Data Health Research: Currents in Contemporary Bioethics.Does peer benefit justify research on incompetent individuals? The same-population condition in codes of research ethics.Inclusion of residual tissue in biobanks: opt-in or opt-out?Clinical research and medical care: towards effective and complete integrationPrivacy revisited? Old ideals, new realities, and their impact on biobank regimesDuty, desire or indifference? A qualitative study of patient decisions about recruitment to an epilepsy treatment trial.Harms, benefits, and the nature of interventions in pragmatic clinical trials.Patients' charters and health responsibilitiesFacilitating the ethical use of health data for the benefit of society: electronic health records, consent and the duty of easy rescue.A critique of the regulation of data science in healthcare research in the European Union.Viewing research participation as a moral obligation: in whose interests?The ethics of unlinked anonymous testing of blood: views from in-depth interviews with key informants in four countries.Risks of phase I research with healthy participants: A systematic reviewParticipation in biomedical research is an imperfect moral duty: a response to John HarrisIncreasing enrollment in drug trials: the need for greater transparency about the social value of research in recruitment efforts'Not taken in by media hype': how potential donors, recipients and members of the general public perceive stem cell research.The obligation to participate in biomedical research.Offering payments, reimbursement and incentives to patients and family doctors to encourage participation in research.Participants' responsibilities in clinical research.Varying ethics rules in clinical research and routine patient care--research ethics committee chairpersons' views in Finland.Children and biobanks: a review of the ethical and legal discussion.Prisoners as research participants: current practice and attitudes in the UK.Advance consent, critical interests and dementia research.Gene Editing, Enhancing and Women's Role.Regulating Privacy and Biobanks in the Netherlands.Changing perspectives in biobank research: from individual rights to concerns about public health regarding the return of results.High hopes and automatic escalators: a critique of some new arguments in bioethics.Ethical considerations in animal studies.Rescuing the duty to rescue.How to keep high-risk studies ethical: classifying candidate solutions.Consent for research in hyperacute stroke.More guidelines on research ethics?Sharing in or benefiting from scientific advancement?Does consent bias research?Biomedical Big Data: New Models of Control Over Access, Use and Governance.
P2860
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P2860
description
2005 nî lūn-bûn
@nan
2005 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
2005 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
2005年の論文
@ja
2005年論文
@yue
2005年論文
@zh-hant
2005年論文
@zh-hk
2005年論文
@zh-mo
2005年論文
@zh-tw
2005年论文
@wuu
name
Scientific research is a moral duty
@ast
Scientific research is a moral duty
@en
type
label
Scientific research is a moral duty
@ast
Scientific research is a moral duty
@en
prefLabel
Scientific research is a moral duty
@ast
Scientific research is a moral duty
@en
P2860
P3181
P356
P1476
Scientific research is a moral duty
@en
P2093
P2860
P304
P3181
P356
10.1136/JME.2005.011973
P577
2005-04-01T00:00:00Z