Data Management

Best Practices in Data Management for Clinical Trials: Ensuring Accuracy and Compliance

Data in clinical trials encompass a comprehensive set of information collected during the study, including participant demographics, medical history, treatment outcomes, adverse events, and other relevant measurements. Those data are recommended to be of high-quality, accurate, align with protocol specifications, and meet regulatory standards. It should exhibit an acceptable level of variation that doesn’t impact study conclusions during statistical analysis. Adherence to protocol requirements is crucial to ensuring the reliability and integrity of the data throughout the trial.

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