Resource Library

eConsent regulations vary widely across the world. Download this guide for an overview of the current regulatory situation in nine countries.

Join this webinar to understand how eConsent works, where it falls in the regulatory guidelines & see a practical demonstration of eConsent software.

Hoboken, New Jersey: September 2, 2020: Castor, a leading provider of clinical trial technology that automates the research…

With 4,000 live studies and 2M enrolled patients across 90 countries, Castor will use the funding to further…

When the COVID-19 pandemic began, the industry needed to focus immediately on research continuity and determine how to mitigate the impact on clinical trials while protecting participant safety.

Download this white paper to learn why patient-centric, remote research technologies such as eConsent, EDC, and ePRO are critical during COVID-19 and beyond.

In 2020, the SARS-CoV-2 coronavirus has infected millions and resulted in death for hundreds of thousands. It has…

The world may have changed seemingly overnight, but clinical research and medical innovation must continue now more than…

Watch this webinar for tips on how to ensure research continuity during COVID-19 by running your trial with…

Clinical trials are experiencing significant disruption worldwide due to the COVID-19 pandemic. Medical research is not immune to…