White Paper

Control Your Data Flow, Control Your Trial

Source: IQVIA Research & Development Solutions

The flood of data pouring into the healthcare industry is creating productivity bottlenecks and introducing new risks that can delay projects and put patient safety at risk. To adapt, life sciences firms need to rethink their entire data ecosystem, adding new technology and talent to transform all that raw data into usable insights. But unless organizations figure out how to capture, integrate, analyze and share these data assets, it could also bring their clinical research to a screeching halt

Consider COVID vaccine trials. During the pandemic sponsors were tasked with recruiting thousands of patients in a matter of weeks, monitoring their outcomes in near real time, and delivering a constant stream of results to regulators. It meant they needed to be able to capture and analyze billions of data points within extremely short timelines. If they hadn't had an effective system to capture and analyze all of that data, the trial workflow would have ground to a halt, adding months to the review process, and delaying access to life saving vaccines. It's one example of the constant pressure every clinical trial team faces.

Read this essential whitepaper and learn from our data management experts on how controlling your data flow can ensure you keep control of your trial.


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