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자료유형
학술저널
저자정보
저널정보
한국재산법학회 재산법연구 재산법연구 제24권 제1호
발행연도
2007.1
수록면
377 - 411 (35page)

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Secondary Uses of Human Biological Materials and Informed Consent Lee, Jae-Mok Informed consent has been at the heart of medical ethics in the modern era. In fact, one could argue that the emergence of informed consent is the hallmark of the modern era in medical ethics. The informed consent concept emanates from the principle of autonomy and envisions a shared, interactive decision-making process. Autonomy is understood as a cluster of notions including self-determination, freedom, independence, liberty of choice and action.Legally valid informed consent is mandated in the clinical sphere for diagnostic and therapeutic, as well as research-related, interventions.However, in addition to exercising the right to make choices about which diagnostic or screening tests therapeutic procedures or medications, and research protocols to undergo or participate in, individuals increasingly enjoy (or are confronted with, depending on one's perspective) other, non-clinical decisions that may well affect their health care deeply.While the socio-ethical and legal issues surrounding secondary uses human biological materials have long been the subject of international interest, the thorny questions of genetic research and biobanking are more recent. Add to this the fact that national guidelines and laws usually precede international policymaking, and the delay in international approaches is understandable. This article examines informed consent requirements for use of stored human biological materials and explores specific approaches for reconciling the informed consent requirements for banked-specimen research under regulations.

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