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Home » U.S. FDA Pressing Trial Sponsors to Go Digital in Case Report Forms
U.S. FDA Pressing Trial Sponsors to Go Digital in Case Report Forms
October 8, 2013
The U.S. Food and Drug Administration is leaning on sponsors to convert from paper to electronic capture of clinical trial source data, saying the change should help eliminate unnecessary duplication of data and transcription errors and promote real-time access to data for review.
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