Castor

Run your EU MDR PMCF program on one platform

How device teams run the whole post-market clinical follow-up program on Castor, from cohort to long-term follow-up.

What is inside

PMCF is a multi-year evidence commitment and the post-market clinical follow-up component of your EU MDR post-market surveillance obligations, expected for most devices unless you can justify it does not apply. This fact sheet shows how device teams run the whole program on Castor: build the cohort, enroll and re-consent patients remotely, pull the retrospective record with AI-driven chart review and human review, and automate long-term follow-up, alongside your sites and partners where the design needs them.

Run the whole PMCF program on one platform, from cohort to long-term follow-up
Retrospective plus multi-year prospective data collected together
AI-driven chart review with human review, human-in-the-loop by design
The scale: 298 post-market studies to date, including PMCF, and 1.27M+ ePRO datapoints