Electronic Patient Reported Outcome (ePRO)

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…

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

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…

Patients suffering from arthralgia at risk of an inflammatory rheumatic disease depend on an appropriate referral. But general…