Assess the protocol against real world evidence using advanced analytics and reduce the risk of costly amendments.
Leverage a global network of Phase I clinical pharmacology units to build diversity in patient populations and access a range of geographic regions for early clinical development programs.
Improve the performance of the clinical trials with the power of IQVIA CORE.
End to end trial management customized to your needs and delivery model. We ensure optimal agility, quality and efficiency in each step of the way.
Connecting to the powerful network that eliminates lag time, expedites startup and maximizes GCP compliance downstream.
Enhancing retention by reducing the patient burden, reducing screen-fail rates and increasing inclusion of traditionally underrepresented population.
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