Clinical trial feasibility often suffers from inefficiencies, inconsistent data, and site overload, delaying recruitment and increasing costs. IQVIA outlines four strategies to improve predictability. First, sponsors should share detailed information and collaborate with sites to refine recruitment plans and identify realistic patient pathways. Second, adopting site-centric partnerships and networks enhances protocol design and performance. Third, leveraging AI and feasibility technology standardizes surveys, improves site selection, and reduces administrative burden. Finally, flexible service models, such as Clinical Trial Educators and research assistants, boost recruitment and ease site workload, accelerating trial success.

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