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In the latest Genome Guidelines revised in 2013, ERCs play a more crucial role in several key decisions on the scope of informed consent, the use of existing samples and the return of research results to sample donors.
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Although a full review on placebo is beyond our scope, two aspects are important: the ethical issues when considering the use of informed consent and the statistical/methodological importance of placebo in clinical trials.
Since then, the notion of informed consent has supported the right of participants in self-determination, and the scope of its application has expanded alongside the dramatic advances in biomedical and clinical research.
§ 16.117 Documentation of informed consent.
§ 225.117 Documentation of informed consent.
§ 431.117 Documentation of informed consent.
Which raises the question of informed consent.
A history and theory of informed consent.
A variety of interventions can enhance understanding of informed consent.
It also requires an evaluation of informed consent procedures.
"It goes to the whole issue of informed consent.
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