IQVIA site support services complement your trial recruitment efforts, allowing sites to focus on high-quality patient care, maximizing patient flow for increased efficiency while continually monitoring staff needs. Having a deep partnership with sponsors and study sites offers not just fast recruitment but quality recruitment, ensuring a first class trial experience.
Decrease clinical development costs and increase study quality using our global functional resources and flexible services, and get more value from your R&D spend.
Predict enrollment more accurately and increase the number of patients per site using data-driven patient recruitment solutions.
Change the model of clinical research by integrating data, expertise, analytics and technology from study design through execution to power better decisions.
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.
