08.07.25 -- Strategizing And Implementing Your Clinical Trial Technologies

Post-marketing signals and AE frequency comparisons need careful interpretation. Discover how confounding factors and misunderstood statistics often mislead drug safety professionals.

TrialKit addresses data management issues in clinical trials through its innovative ePRO and eCOA tools, which facilitate real-time data collection and reporting.

In this comprehensive guide, IQVIA's eCOA library and licensing specialists, Kayla Doyle and Piero Bindi, explore five essential steps for obtaining licenses for the assessments required in your clinical trial.

Uncover how an independent confirmation of compliance opened up new opportunities and is instilling confidence in customers who are integrating the eSource system into their software validation strategy.

In this 4-part series, learn about AI-driven methods that streamline data mapping and highlight critical issues that allow clinical teams to focus on what truly matters.

This study evaluates to what degree an eSource-to-EDC data transfer initiative succeeds through two key dimensions: "Mappability" and "Prevalence".

Learn how you can leverage a system that offers flexible data delivery formats and seamless integration into commercialization workflows while also ensuring HIPAA-compliant de-identified data.