What is the difference in EHR's involving the terms "Subject" and "Patient" in regards to clinical research data aggregation? Also, what are the legal ramifications of involuntary subjugation of private citizens to clinical research PI's? Why won't the research community discuss such probabilities?
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What is the difference in EHR's involving the terms "Subject" and "Patient" in regards to clinical research data aggregation? Also, what are the legal ramifications of involuntary subjugation of private citizens to clinical research PI's? Why won't the research community discuss such probabilities?