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The Methodology of the Collection of Adverse Event Data in Clinical Trials

  • M. D. B. Stephens
Chapter

Abstract

In order to collect ADR efficiently, it is necessary to know which factors might hinder their collection so that these can be circumvented. Between the advent of an adverse event and its final assessment as an ADR the adverse event must be communicated. The factors preventing this communication are as follows.

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© M.D.B. Stephens 1988

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