Delve Health Provides the Technology Platform to Design Clinical Trials to Fit a Patient’s Lifestyle
What is eConsent
Defining eConsent in Clinical Trials The US Food and Drug Administration (FDA) has defined electronic informed consent (eConsent) in clinical trials as “the use of
Opportunities In Transforming Clinical Research In The US
Clinical trials are essential for the development of new drugs and treatments. The goal of clinical trials is to find better ways to prevent, diagnose,
For A Monkey Pox Treatment: US Government Shows Initiative
The United States government is no stranger to being proactive when it comes to outbreaks of deadly diseases. In the face of a potential monkeypox
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 was
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 internet.”