Full service R&D Capabilities
IQVIA’s CORE™-enabled approach to Clinical Development - from design to delivery
We share your vision to drive healthcare forward – and we can help you accelerate your achievements. We’re bringing together human data, data science and human science to harness advances in technology, analytics and human ingenuity and enable you to fast forward your clinical development.
Take full advantage of new opportunities to optimize your R&D efforts. IQVIA’s full-service clinical development capabilities can help you significantly reduce timelines, lower costs, reduce oversight, and improve time and budget predictability.
- Expand your development capabilities. IQVIA’s full-service offering provides institutional expertise, innovative technologies and advanced analytics powered by the IQVIA CORE™. With integrated and proven processes for project management, clinical monitoring, data management, biostatistics, safety, medical writing, regulatory affairs, document publishing and more, you get the support you need to advance human health.
- Gain scalable best-in-class experience to supplement your expertise. We have executed more clinical trials than any other organization in the world. The largest pharmaceutical firms in the world, and emerging biotech companies, have leveraged our full-service CRO capabilities.
- Get measurable results. IQVIA can help you start up oncology sites as fast as 21 days, reduce non-enrollers up to 18%, and increase recruitment rates by up to 21%. You’ll gain increased predictability in timelines and budgets.
We’re committed to providing solutions that enable you to innovate with confidence, maximize your opportunities, and, ultimately, drive healthcare forward.
Let us help you optimize you clinical trial from design to delivery.