Question:
(1) disclosure of information, (2) competency of the patient (or surrogate) to make a decision, and (3) voluntary nature of the decision. US federal regulations require a full, detailed explanation of the study and its potential risks
Author: Paul HogueAnswer:
What should be included in an informed consent?
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Paul Hogue![Paul Hogue](https://markdown.memory.com/static/anonymous.png)