IQVIA’s Clinical Data Analytics Solutions (CDAS) helps you solve key challenges such as oversight, data management and clinical trials process automation. CDAS uses modern technologies to consolidate data, accelerate review, and improve time to analysis and insights. And with the use of AI, it automates clinical trial processes by generating intelligent insights.

CDAS helps you harness clinical research data in a single ecosystem. Generate smarter insights augmented by AI. And drive intelligent action to transform clinical outcomes. CDAS delivers flexible solutions aimed at solving challenges like these three critical examples, by combining the power of data and modern technology.

• First, Clinical Trial Oversight. What if you could feel confident that you are meeting regulatory expectations for sponsor study oversight even in an outsourced model where your data sits with multiple CROs and other vendors? CDAS enables you to reduce the manual effort of collecting and compiling data from multiple vendors, in disparate formats, and at varying cadences. Get your data in your hands in near real time, standardized across vendor sources. Manage clinical trials across your entire portfolio with comprehensive, intelligent analytics.
  
  The result: Spend less time compiling data and more time analyzing data insights for higher quality oversight and more proactive risk management.
• CDAS also delivers comprehensive tools to address common data management challenges. Today’s modern clinical trials mean source data is captured in multiple systems. It’s not just an EDC world anymore. And conducting data reviews across disparate systems is not a realistic option. What if you had an easier way to ensure clean, high-quality data in trials where 70 percent or more of your data is in a non-EDC source? CDAS addresses this challenge by first consolidating the data, then facilitating review. Collaborative review of data across data management, medical, and safety functions leads to more efficient management of issues and ultimately to a reduced number of redundant queries sent to the site. Using AI-automated quality checks and recommended corrective actions helps identify anomalies in seconds versus days.
  
  The result: Increased data accuracy, timeliness, and quality, ultimately leading to your ability to achieve faster database lock and submission readiness.
• And finally, take control of massive trial document volumes with Intelligent Document Review. What if you could manage document quality and automatically index your study documents where they belong in the eTMF with 99 percent accuracy? IQVIA Intelligent Document Review does all this heavy lifting for you. IQVIA Intelligent Document Review harnesses the power of AI to curate, quality check, digitize, and classify documents, with a flexible, seamless tool, ready to work with any eTMF.

IQVIA's Clinical Data Analytics Solutions provides a modern, AI-driven clinical data ecosystem for stakeholders to investigate operational and clinical data, perform machine-augmented analytics, and drive better research outcomes.

Contact us today to learn more about CDAS and other solutions in our Orchestrated Clinical Trials platform.