Trial data should be cleaned and standardized throughout the study instead of only at study close-out.
TORONTO, Ontario (PRWEB) May 18, 2020
Clinical Data Management (CDM) has the important role of ensuring high-quality, reliable and statistically sound data across all clinical trial phases. Yet, the process is more complex than a simple review of the data. Trial data should be cleaned and standardized throughout the study instead of only at study close-out.
To efficiently accomplish quality data review in a timely manner, a comprehensive data management ecosystem is essential. Such an ecosystem incorporates an experienced team, best-practice guidelines, standard templates, medical coding tools, standard operating procedures and more. In addition, seamless integration between electronic data capture (EDC) and other systems simplifies the data management process.
For more information or to register for this event, visit Simplifying Clinical Data Management With a Comprehensive Ecosystem.
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