Medical device clinical trial platform one-pager

The Castor platform for medical device trials, on one page

A shareable summary of how device teams run studies from first-in-human to post-market on Castor.

The device teams on Castor span cardiovascular, orthopedics and MSK, surgical and interventional, neurology and neuromodulation, and digital health and SaMD.

What is inside

Legacy EDCs are overkill for lean device studies, and evaluating platforms takes weeks your team does not have. This one-pager gives your team and your stakeholders the whole picture on a single page: what Castor does for device studies, the numbers behind it, and where AI-driven extraction changes the work. Built for forwarding to the colleague who asks what you are evaluating.

The platform in brief: EDC, ePRO, and eConsent in one validated environment
Catalyst Site Upload: sites submit surgical notes and worksheets, no EDC training for data entry
PMCF under EU MDR: registry, survey, and chart-review designs with audit-ready exports
The scale: 900+ device studies to date, 320,000+ patients, 5,200+ sites
Proof: MMI, Sword Health, and the human-in-the-loop error rate