good practice In informed cansent procedure with regards to documentation which one of the not good practice?
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What are the best practices of creating an informed consent?
Valid informed consent for research must include three major elements: (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.
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