Effortlessly conduct multi-center clinical trials worldwide for drug development with Castor’s EDC and CDMS platforms, including eCOA, ePRO, EHR eSource, eConsent, and IRT modules.
Boost site/patient discussions and clinical trial efficiency while experiencing a more reliable way to consent patients into a clinical trial with electronic consent forms.
With robust APIs, detailed guides, and real-time monitoring, Signant SmartSignals Marketplace enhances eClinical workflows, minimizing duplication and ensuring reliable data across systems.
Uncover how the Signals Clinical platform successfully enables the rapid delivery of clinical insights that inform both clinical and operational study decisions.
Explore the interconnected data flow across Veeva Vault EDC, Veeva CDB, Veeva RTSM, and Veeva ePRO to visualize how these products work together seamlessly.
Dive deep into the capabilities of IQVIA's eCOA with expert Edward Bartels as he demonstrates how to easily create diaries, schedule assessments, and manage translations and compliance.
Discover why more life science teams are using OpenClinica Unite to automate source data acquisition from patient medical record systems to clinical trial research databases and case report forms.
