IQVIA’s Statistical Programming team delivers automation across the clinical trial analysis process, reducing cycle times and ensuring regulatory compliance. Experts in CDISC standards, they provide dataset development (SDTM, ADaM), legacy conversions, PK/PD analysis, safety reporting, pooled submissions, and key regulatory deliverables. With 1,100+ programmers—70% having 5+ years’ experience—IQVIA offers both full-service and FSP models. Services include structured communications, training, planning, resourcing, and governance, ensuring efficient, high-quality results. Leveraging tools like SAS, R, and WinNonlin, IQVIA expedites submissions while maintaining rigorous quality and compliance.

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