Home » Sponsors Should Plan Ahead to Deal With Missing Data
Sponsors Should Plan Ahead to Deal With Missing Data
To avoid problems with missing data in clinical trials, sponsors should identify, before beginning a trial, methods to account for planning, conducting or analyzing results of a confirmatory study, according to a final guideline recently released by the European Medicines Agency. The guideline, effective Jan. 1, focuses on data missing due to patients withdrawing from a trial and provides frameworks for handling the problem.
Clinical Trials Advisor
Clinical Trials Advisor
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