Browsing by Keyword "informed consent"
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The History of the Informed Consent Requirement in United States Federal Policy
(2001)The informed consent provision in United States federal policy serves a crucial function by protecting human subjects participating in medical research experiments. This paper will trace the development of informed consent ... -
Implementation of Electronic Consent at a Biobank: An Opportunity for Precision Medicine Research
(MDPI, 2016)The purpose of this study is to characterize the potential benefits and challenges of electronic informed consent (eIC) as a strategy for rapidly expanding the reach of large biobanks while reducing costs and potentially ... -
"Informed" Consent and Human Experimentation: Present Status, Pitfalls, and the Need for Reform
(2001)To demonstrate the inadequacies of informed consent in the contemporary context and the need for better subject protection, this paper begins by scrutinizing the rise of modern informed consent doctrine in international ... -
Research on the Terminally Ill: A Balancing Act Between Facilitating Access to Innovative Therapies and Protecting Vulnerable Subjects in Search of One Last Hope for Survival
(2003)This paper presents the application of the current federal regulatory system governing clinical research in the United States to research involving terminally ill subjects, with a special emphasis on those patients battling ... -
Scientific tools, fake treatments, or triggers for psychological healing: How clinical trial participants conceptualise placebos
(Elsevier BV, 2012)Placebos are an essential tool in randomised clinical trials, where they are used to control for contextual healing effects. Placebos and their effects are also studied from multiple diverse perspectives, but the perspectives ...