Electronic Patient Reported Outcome (ePRO)

Castor’s ePRO solution enabled AKRN and Company Z to engage with a participant population that, on their own, might struggle with a technology solution that they’ve never used before.

AKRN Scientific Consulting, a medical device CRO, used Castor’s flexible EDC solution to handle constant mid-study changes for their client.

Castor is shifting the research paradigm for eCRF in clinical trials, transitioning from old, inefficient processes to a comprehensive CDMS & DCT platform.

Castor explores how clinical researchers improve the participant experience by having good user design in their patient-facing technology

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…