Abstract
In recent years, biobanks have become major strategic and powerful tools for undertaking medical-scientific research. However, the use of human tissue and donor-related data for research and biomedical applications raises important legal and ethical questions. In this article, I focus on the concept of informed consent, an issue that has advanced to become one of the most contested issues in biobanking. Much has been written in recent years to address the challenges connected to research biobanks and informed consent, in particular with regard to various consent models discussed by legal and ethics scholars, but the issues are still far from being solved. In a second part, I will discuss the role of informed consent within utilitarian and human rights approaches and its implications for human nature. I argue that a clear commitment to a human rights approach should be adopted, one that values and respects the individual as the sample donor and asks for his/her informed consent in cases where his/her bodily material will be used for current and future research.
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Dörr, B.S. (2014). Collection of Human Tissue Samples in Biobanks: Challenges to Human Rights and Human Nature. In: Albers, M., Hoffmann, T., Reinhardt, J. (eds) Human Rights and Human Nature. Ius Gentium: Comparative Perspectives on Law and Justice, vol 35. Springer, Dordrecht. https://doi.org/10.1007/978-94-017-8672-0_13
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