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Efficient patient enrollment is a cornerstone of clinical trial success, directly impacting budget and patient access to new therapies. However, approximately 80% of clinical trials fail to meet initial enrollment targets, leading to delays, cost escalations, and regulatory challenges.
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Discover how integrating internal and external data can enhance decision-making and efficiency, how to manage diverse data sources, and the benefits of a single source of truth for your organization.
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Rare disease clinical trials face distinct challenges due to small, geographically dispersed patient populations, limited historical data, and a scarcity of experienced investigators. TA Scan’s clinical intelligence platform offers a transformative approach to addressing these complexities, enabling sponsors to enhance enrollment strategies.
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Effective trial feasibility and enrollment planning are critical to the success of clinical research. However, the complex interplay of factors such as regulatory timelines, patient recruitment rates, site capacity, and competing trials often complicates the process. TA Scan’s Trial Feasibility Flex addresses these challenges.
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