Resource Library

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…

In this webinar, we explain how to do the following: Use variables in your study to calculate scores…

In this webinar, we answer the following questions: Am I allowed to store personally identifiable information in my…

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.

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

In this webinar, we discussed how to build your study form (eCRFs) on Castor EDC as well as…

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

Under the MDR, PMCF activities will be mandated as part of medical device surveillance programs. These activities should…