11.26.24 -- Where AI And Regulation Meet

Consider several forward-looking strategies shared by industry leaders that can also serve as a valuable resource for professionals navigating the complex terrain of clinical research collaboration.

Duke’s new research shows why participants prefer an eConsent experience bolstered with videos, media, questions, and more.

Which factors should you consider when selecting an IRT/RTSM vendor to ensure your trial's randomization and supply management processes are successfully executed?

A simulated study has showcased the benefits digital biomarkers could have on the future of trial durations and sample sizes for clinical trial sponsors.

See firsthand how this modern build platform, which includes a ‘one-click’ library of pre-validated questionnaires, reduces build times by 75% and means mid-study updates can be actioned in minutes.

Gather data directly from the patient—the true source. Empower your team to streamline data collection, making it faster and easier for everyone involved.

Dive deep into the capabilities of IQVIA's eCOA with our expert Edward Bartels. He will focus on how to effortlessly create a diary, schedule site/participant assessments, and intuitively manage translations and compliance.