Mariam F. Eskander, MD, MPH, and Coral O. Omene, MD, PhD, discuss how medical mistrust has impacted participation in oncology clinical trials.

Biomedical concepts by CDISC are tailored to ensure data consistency, and link information throughout the data pipeline.

Florence has been issuing its State of Technology Enabled Clinical Trials Report for five years now, so there is contextual ...

Thinking about participating in a clinical trial? Here are 15 questions to ask your doctor about clinical trials for you make ...

University of Cincinnati experts will present research at the International Stroke Conference 2025 in Los Angeles.

A 2024 survey of eCOA professionals at sponsor organizations revealed that 50% of respondents identified eCOA Data Change ...

Kevin Curtis, managing director of Driving Monitor, explained: “Our new eConsent system is called ePass (Electronic Permit and Safety System) and connects the driver consent with the new live realtime ...

MaxisIT, a leader in AI-powered clinical trial technologies, today announced the release of Site Copilot, the latest innovation built on the cutting-edge DTect AI platform under MaxisIT's Agentic AI ...

Background: Obtaining timely informed consent is a key barrier in acute ischemic stroke (AIS) clinical trial recruitment. Electronic consent (eConsent) allows electronic delivery and documentation of ...

“oomnia has been purposefully designed as a unified solution. Key clinical trial management tools, including EDC, RTMS, eTMF, CTMS, eConsent, ePRO and eSource, are integrative parts of the same ...

The company's suite of solutions, including CDMS/EDC, eCOA/ePRO, eConsent and RTSM, enables the capture of quality clinical trial data while optimizing workflows for regulatory readiness.