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  1. Spanish Regulation of Biobanks.Pilar Nicolás - 2015 - Journal of Law, Medicine and Ethics 43 (4):801-815.
    Spain occupies an area of 504.645 km, and it has a population of 46.5 million people, out of which 4,538,503 are immigrants. Life expectancy is 82.5 years. Its economy grew 1.4 % in 1014. Its current Constitution was enacted in 1978. It has been part of the European Union since 1986. Spain is a social and democratic state subject to the rule of law. Liberty, justice, equality, and political pluralism are the highest values of the legal order of the rule (...)
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  • The role of research ethics committees in South Africa when human biological materials are transferred between institutions.S. Mahomed & M. Labuschaigne - 2019 - South African Journal of Bioethics and Law 12 (2):84.
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  • A framework for ethics review of applications to store, reuse and share tissue samples.Ian Kerridge, Cameron Stewart, Wendy Lipworth & Shih-Ning Then - 2021 - Monash Bioethics Review 39 (1):115-124.
    The practice of biobank networking—where biobanks are linked together, and researchers share human tissue samples—is an increasingly common practice both domestically and internationally. The benefits from networking in this way are well established. However, there is a need for ethical oversight in the sharing of human tissue. Ethics committees will increasingly be called upon to approve the sharing of tissue and data with other researchers, often via biobanks, and little guidance currently exists for such committees. In this paper, we provide (...)
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  • Marking Shifts in Human Research Ethics in the Development of Biobanking.D. Chalmers, M. Burgess, K. Edwards, J. Kaye, E. M. Meslin & D. Nicol - 2015 - Public Health Ethics 8 (1):63-71.
    Biobanks are increasingly being created specifically for research purposes. Concomitantly, we are seeing significant and evolving shifts in research ethics in relation to biobanking. Three discrete shifts are identified in this article. The first extends the ethical focus beyond the protection of human subjects to the promotion of broader community benefits of research utilizing biobanked resources, and an expectation that these benefits will be shared. The second involves the evolution of the traditional consent paradigm for future research uses of biobanks (...)
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