Better outcomes backed by deeper expertise.

The right insights help deliver the right outcomes – faster and more efficiently.

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.

The biostatistics team at IQVIA is experienced in submissions in all major regions, working together with key groups like Global Regulatory Affairs, Safety, Project and Data Management, and Medical Writing to drive efficiency and accountability.

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Innovation - driven insights 

Using the IQVIA CORE, we leverage advanced analytics and innovative technologies to enhance clinical expertise and turn data into power for our customers.

Working with emerging biopharma firms and global pharmaceutical manufacturers alike, we deliver the trial performance analytics and timely insights you need to make decisions that benefit your patients.

Advanced technology drives pharmacology modelling and simulation, adaptive designs, comparative analysis and population identification, while clinical data analysis fuels clinical trial success, from planning stages through execution to reduce costs and risks, while accelerating timelines and improving quality of submissions.

IQVIA CORE + Biostatistics = Science and Production

Broadly speaking, biostatistics encompass science and production activities required to summarize and analyze the data collected in clinical research and trials. Biostatistics are used to interpret and draw inferences from data collected on subjects as they progress through a trial and serves as the bridge between data capture and reporting.

  • Designing your study – leverage expertise in modeling and simulation, adaptive trial design, consulting services, and feasibility analysis
  • Evidence collection – optimize protocol and CRF development, biomarkers and early clinical decisions, statistical analysis plans, and data visualizations
  • Filing and registration – SDTM and AdaM, integrated analyses, regulatory submission support and representation, and expert testimony
  • Maximize commercial success – Post-marketing manuscript support, Pharmacoeconomics, competitive analysis, and commercial marketing


Better design leads to better outcomes

Seasoned biostatisticians apply deep regulatory knowledge to help you navigate the complexities of study design, including endpoint selection, sample size, analysis methods, and data displays and interpretations, providing speed and flexibility with study reporting.

All therapy areas and indications benefit from biostatistics services. Biostatisticians collaborate with key groups at every stage during a development program to provide a breadth of services which enhance the overall success.

Full service and standalone

IQVIA also offers biostatistics and pharmacokinetics within custom Functional Service Provider (FSP) and standalone solutions to meet specific needs.

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Engage early to maximize benefits

Early Biostatistics engagement can help identify gaps in your development strategy and in individual protocols. This often helps avoid errors and sidestep costly delays or inaccuracies that may cause regulators to challenge their marketing applications.

IQVIA Biostatistics can determine the best path forward for products before a trial begins, saving you time and money through scientific expertise which can also alleviate regulatory concerns.

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