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Titlebook: Ethics and Governance of Biomedical Research; Theory and Practice Daniel Strech,Marcel Mertz Book 2016 Springer International Publishing Sw

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樓主: Halloween
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發(fā)表于 2025-3-23 13:37:55 | 只看該作者
12#
發(fā)表于 2025-3-23 15:35:29 | 只看該作者
https://doi.org/10.1007/978-3-658-37774-8ssent has been about the necessary conditions for making a morally significant decision. Some argue that to make a morally significant decision a child has to understand the abstract concept of altruism. Therefore it is crucial to determine at what stage of development this ability arises. Others ar
13#
發(fā)表于 2025-3-23 20:33:29 | 只看該作者
Einleitung. Fixierung der Probleme,of phase IV studies has led to a greater need to examine the applicable ethics at this stage. Building on our previous work on ethics in phase IV studies, we propose that the following ethical principles are indispensable to implementing ethics in phase IV: (A) When discussing the possibility of wai
14#
發(fā)表于 2025-3-23 23:17:07 | 只看該作者
Die mathematisch begründeten Ergebnissee Research Ethics Committee of the University of Freiburg, Germany. Published full articles were searched in electronic databases and investigators contacted. Data on study characteristics were extracted from protocols and corresponding publications. We characterized the cohort, quantified its publi
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發(fā)表于 2025-3-24 04:16:15 | 只看該作者
16#
發(fā)表于 2025-3-24 10:07:51 | 只看該作者
https://doi.org/10.1007/978-3-322-92512-1te of delivery. Typically, these conditions are discovered over the course of early phase clinical testing. In what follows, we describe a conceptual tool—“ensemble space”—for understanding scientific decision-making in the early phases of clinical development. Briefly, we liken each condition to a
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發(fā)表于 2025-3-24 12:56:45 | 只看該作者
18#
發(fā)表于 2025-3-24 18:36:47 | 只看該作者
,Optionsscheine und B?rsentermingesch?fte,d. Three popular interpretations of the minimal risk threshold and the problems they raise when applied in the research context are presented. First, the “risks of daily life” standard and the “routine examinations” standard are addressed. It is argued here that neither of them can provide a satisfa
19#
發(fā)表于 2025-3-24 22:30:53 | 只看該作者
https://doi.org/10.1007/978-3-642-94447-5ity) is relatively new, and it is taking place at a time when the possibility of undertaking quite detailed genotyping and sequencing is assuming much greater prominence. Although there is much to debate concerning such biobanks, there is broad agreement that their good governance and legitimacy hin
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發(fā)表于 2025-3-25 01:01:15 | 只看該作者
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