Data sharing among data monitoring committees and responsibilities to patients and science
Over the past three decades it has become increasingly recognized that systematic assessment of as high a proportion as possible of relevant research evidence is needed to protect the best interests of patients and the public. For example, this principle is manifested in clinical guidelines and, inc...
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Veröffentlicht in: | Trials 2013-04, Vol.14 (1), p.102-102 |
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Sprache: | eng |
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