07.22.25 -- Are Sites Even Using AI? How Sponsors And CROs Can Support Uptake

Our electronic CDRS-R doesn't just digitize the scale. It embeds clinical expertise, automates quality controls, and guides raters through every step to ensure consistent, reliable data.

Explore how an eSource approach to clinical trial data can reduce site burden, eliminate double data entry, minimize queries, and enhance remote monitoring.

The I-SPY 2 Trial represents a groundbreaking approach in oncology, with a key component of the trial's success being the integration of EHR with EDC via a unique platform.

Discover an easy-to-use platform to centralize RFPs, budgets, and vendor data so you can select the right partners, manage change orders, and keep your studies on track.

More than just a builder, Medable Studio offers unmatched control over study creation and launch, eliminating the common roadblocks of study startup and empowering users throughout the process.