08.12.25 -- 5 Best Practices For Improving AI Literacy In A GxP Environment

The CDISC + TMF Europe Interchange showcased critical insights for TMF professionals. Learn about essential collaboration, the impact of AI, and the continued drive for standardization in clinical trials.

Central eSource transforms data capture from a passive, back-end chore into an active, real-time quality and compliance engine—delivering benefits that extend beyond faster EDC feeds and reduced SDV.

Whether you're a sponsor, site, or technology vendor, now is the time to embrace One Home and join this industry-wide collaboration.

For scalable CNS trials, central rating models offer a way to standardize data collection globally while enhancing patient accessibility and inclusion.

Join industry leaders from Anju and 9 Labs for a presentation on the pivotal role of Strategic Communication Plans (SCP) in medical affairs.

Ensure seamless, accurate global study translations and efficient localization with IQVIA eCOA, leveraging our proven vendor relationships and streamlined process to keep your study on track.

This dynamic, system-agnostic approach to modernizing clinical trial monitoring supports targeted oversight, as well as sampling at the subject, visit, and form levels.