IQVIA Global Clinical Data Management

The value of data is derived from it being accurate and timely. As today's clinical trials rely on and generate massive amounts of data, sponsors rapidly turn to third party data sources to collect key study data in large volumes. It is critical for you to bring siloed data together in a meaningful way, ensuring the transparency, integrity and quality of your data are optimized to better guide your decision making.

The experienced IQVIA Global Data Management team provides innovative, end-to-end solutions for the management and delivery of high-quality, integrated, timely data in Phase I-IV trials.

Data Management

Ensure you have access to insights early with connected devices and clean, analysis-ready data

Phase IIb/III Trials

Improve the performance of your clinical trials with the power of the IQVIA CORE.

Clinical Trials

Change the model of clinical research by integrating data, expertise, analytics and technology from study design through execution to power better decisions.

Clinical Research & Development Solutions

Explore our end-to-end, full service clinical development capabilities including Therapeutics expertise, Development Planning, Phase I early clinical development, Phase IIb/III and Phase IV Trials, Regulatory Submission and Post-Launch Studies.

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