Take a moment to watch this animated video, and you will get an engaging sense of how IQVIA Precision Enrollment can help reduce your study start up by opening sites to studies only when they have a qualified patient.
The right sites. The right patients. Within 21 days. Total Run Time: 1:54 minutes.
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.
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.
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