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Informed consent

Executive Summary

FDA and NIH will hold a "Public Forum on Informed Consent in Clinical Research Conducted in Emergency Circumstances" Jan. 9-10 at the Bethesda (Maryland) Marriott. Emergency-care specialists have complained that existing informed-consent regulations do not account for situations in which there is no time to spare and the potential subjects are physically or mentally unable to give meaningful consent. The forum will feature discussion of the current regulations and the distinctive elements of emergency-research protocols, and presentation of case studies. Public testimony will be heard Jan. 10
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