Companies are looking to create a data flow process to reduce the time between last patient, last visit, and submission. Standards, specifically CDISC and FDA Guidelines, provide a foundation to operating a data flow process. Combined with central data storage system, time to delivery can be reduced to days.
The use of standards is not new, but holding to a single set of standards can be a challenge. Study teams are faced with new study designs and efficacy analytics. Providing an expert to guide teams in following standards, thereby empowering data flow, is a way to help study teams adjust to changes.
Three key take-aways:
Getting the right outcomes from your clinical trials is all about the data and insights they provide. Biostatistics in clinical trials isn’t just a necessity, it can be a real competitive advantage.
Improve the performance of your clinical trials with the power of the IQVIA CORE.
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