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Science 6 October 1995:
Vol. 270. no. 5233, p. 25
DOI: 10.1126/science.270.5233.25b
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News & Comment

Lori Wolfgang

The Food and Drug Administration and the National Institutes of Health are proposing new procedures that will enable emergency-room physicians to test clinical procedures when it is difficult to obtain a patient's informed consent. They are walking an ethical tightrope.




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Science. ISSN 0036-8075 (print), 1095-9203 (online)