09.15.25 -- [Resources] Your IRT Insights, Videos, and More

Regulatory inspections are becoming more frequent and complex. Discover five steps to strengthen IRT inspection readiness; from audit trails and data integrity to clear roles and team training.

Cell and gene therapy pioneers need supply chain partnerships that mitigate trial risk and complexity. Explore how IRT can optimize pre-trial and pre-screening activities while reducing trial cost and risk.

As early phase clinical trials grow more complex, sponsors are now leveraging flexible IRT solutions to replace error-prone manual processes and gain greater control and efficiency.

In a recent Clinical Leader Live webinar, IQVIA supply chain experts shared strategies to streamline shipments, reduce waste, and provide greater drug accountability. A Q&A session followed, in which the panelists shared best practices for an optimized supply chain.

As part of the inaugural Clinical Leader Solutions Showcase in October 2023, IQVIA's Dan Pavitt highlights the latest innovative techniques — showcasing new capabilities in trial design, delivery, conduct, and monitoring of clinical trials.

See how IRT-powered supply automation uses intelligent algorithms to analyze drug supply data and automatically adjust site-level deliveries to each site based on available IRT data.