This volume addresses the proper character of patient informed
consent to medical treatment and clinical research. The goal is
critically to explore the current individually oriented approach to
informed consent which grew out of the dominant bioethics movement
that arose in the United States in the 1970s. In contrast to that
individually oriented approach, this volume explores the importance
of family-oriented approaches to informed consent for medical
treatment and clinical research. It draws on both East Asian moral
resources as well as a critical response to the ways in which the
practice of informed consent has developed in the United States
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