
RWE is finding a role earlier in drug development than ever before, but the data quality, integration, and organizational alignment required to make it regulatory-grade are still catching up to the ambition.
At the upcoming DIA 2018 meeting, Tufts Center for the Study of Drug Development will preview its study findings on the root causes for delays and inefficiencies impacting trial timelines. Through this study, Tufts spoke with executives to learn about the top challenges and opportunities in clinical data management.
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