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Join experts as they reveal how AI is being used today across feasibility, site selection, and trial strategy, as well as how pairing AI with high-quality, expert-backed data leads to successful clinical research.
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What exactly are the updates to the International Council for Harmonisation’s (ICH) Good Clinical Practice (GCP) guideline? Our FAQ outlines the biggest shift, how it impacts protocol design, how roles and responsibilities change, and much more.
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Discover how a connected approach links feasibility and recruitment, using real-world data to design realistic protocols, reach the right patients, and accelerate enrollment with confidence.
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The number of industry-sponsored clinical studies completed in 2024 saw a remarkable 14.2% increase, the largest jump in eight years. This growth highlights the need for strategic approaches in every part of the drug development lifecycle.
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Sitetrove+ and Trialtrove+ can address challenges in identifying the most suitable trial sites and investigators, optimizing feasibility planning, reducing screen failure rates, and improving patient retention. These solutions help streamline and accelerate clinical trial planning.
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