With our fully configurable ePRO/eCOA solution, we help assure your team gets the highest quality patient-reported outcomes for your study. The movement from paper-based to ePRO data capture has enhanced the integrity and accuracy of clinical trial data and is encouraged by regulators.
We offer flexible, automated notifications and robust patient-reported outcome tools that give you more accurate and complete data. Here are some reasons why our clients utilize our platform, and solutions.
Clinical StudyPal meets all global regulations for collecting clinical trial data including ICH/GCP, 21 CFR, GDPR, and HIPAA.
More about our capabilities – we can utilize home clinical visits (using a network of 1million nurses) and mobile application technology to screen and gain consent from patients using video-conferencing, and allowing nurses to collect data through an app and supply patients with ePROs
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Delve Health Provides the Technology Platform to Design Clinical Trials to Fit a Patient’s Lifestyle—Not the Other Way Around
A significant number of companies announced delays and cancellations to planned and on-going clinical trials because of COVID-19 lockdowns and social distancing measures. There
Remote Patient Monitoring in Clinical Trials
In 1958, AT&T came out with the Bell 101 modem—the first commercial modem to transmit data via what would later be known as “the
Opinion: We Have Been Gifted a New Outlook on Increasing Patient Diversity, Compliance, and Retention in Clinical Trials
ACRP Clinical Researcher—June 21, 2022 Our own co-founder and CEO of Delve Health, Wessam Sonbol was published in the ACRP Clinical Researcher magazine. The
Conversations On the Ground—Traditional CROs vs. Virtual CROs
Delve Health’s upper management is currently attending the Drug Information Association’s (DIA) 2022 Global Annual Meeting in Chicago, Illinois. While we are taking all
Clinical Trials Day
May 20, 2022—Today is Clinical Trials Day. A day to recognize and raise awareness as to why clinical trials are so important to all