Electronic Patient Reported Outcome (ePRO)

Castor advisor Craig Lipset, suggests that you consider DCT technology as three separate tiers. Learn more about these tiers and get started with DCT in 2022 with these pro tips.

Watch this webinar for tips on how to ensure research continuity during COVID-19 by running your trial with a more decentralized approach.

Registry studies focused on a specific medical device are a valuable tool to capture the safety and outcomes of the device over its lifetime. Read more here.

This playbook is a tool for sponsors and CROs who want to leverage DCT technology to support remote interactions in their clinical studies.

This playbook is a tool for sponsors and CROs who want to leverage DCT technology to support remote interactions in their clinical studies.

Patient reported outcome measures in clinical trials have traditionally been done on paper. Surveys are a common way…

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

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.

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

As of early April 2020, over 1,000,000 people have been confirmed infected with the SARS-CoV-2 coronavirus, and governments…