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Set your next oncological clinical trials up for success using high-quality real-world data (RWD) to anticipate and confront potential problems early on. Explore how trial sponsors and CROs can now utilize high-quality RWD-backed protocol design to help assess your trial's feasibility, improve patient representation and eligibility, and more.
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This study challenges exclusionary approaches to clinical trials that underrepresent certain populations and limit the generalizability of research advancements. Using a nationwide electronic health record-derived de-identified database, this study evaluates the effect of broadened eligibility criteria on sociodemographic diversity.
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In the complexity of oncology trials, EHRs have enhanced patient safety and workflow efficiency. Despite these benefits, EHRs can be costly and result in extended timelines. Learn how a hybrid model that leverages specialized health data companies could be a more effective way to streamline the patient screening process.
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Watch Flatiron Clinical Pipe™ In Action
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Learn how you can save time with Flatiron Clinical Pipe™, the leading EHR-to-EDC connector that can transfer structured and unstructured data. Lower your data monitoring costs, accelerate data cleaning timelines, and hit study milestones faster.
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