Patient Perspective of Informed Consent Process in Clinical Studies

| June 19, 2015

Include aspects of therapeutic misconception, patient understanding of information, why do patients sign up for
studies, what are their impressions: Rare disease populations is specific interest in comparison to other non-rare
diseases. Do they sign up for research for different reasons due to pressure to find a cure.

 

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Philosophy of Management
use of digital technology

Category: Uncategorized

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