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…

Download this white paper to prepare for the new MDR requirements requiring that PMCF investigations be conducted in compliance with ISO 14155.

eClinical systems must be flexible and adaptable to keep up with the ever-changing demands of modern clinical trials….

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.

The path to market for medical devices can be fraught with obstacles. One of the first challenges confronted…

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.