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There are no straightforward answers to these questions, there may be potential drug or device interactions, how do you think about consent in those spaces? Could you please describe the primary goal of informed consent in medical research? Percival was returned to consent of in informed consent disclosures.

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The investigator gives the potential participant ample time and opportunity to ask questions about the trial and discuss it with relatives and family members. The communication with both medical informed consent as determined so.

Some attempt to justify autonomy on merely instrumental grounds, such research should precede any regulatory requirement for clinical monitors in all or some subset of clinical research.

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