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.
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.
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.
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.
Navigate complex regulatory requirements with expert insights and bring transparency, efficiency and predictability to your regulatory affairs strategy.
Ensure you have access to insights early with connected devices and clean, analysis-ready data
Improve the performance of your clinical trials with the power of the IQVIA CORE.