What does it take to design a post-market clinical study that actually enrolls?

85% of post-market device studies miss their enrollment timelines — and it's rarely about the science. It comes down to what happens at the site level: coordinators managing a second system, surgeons handed a tablet mid-clinic, patients who never received automated outreach.

In this webinar, PatientIQ's Director of Clinical Research, Alyse Borelli, MPH, CCRP, breaks down what high-performing sites do differently, how EHR-native data collection changes coordinator burden and PRO response rates, and a practical checklist for med device teams designing post-market studies.

Watch the recording to learn how PatientIQ can help your team build a post-market study infrastructure that supports enrollment from day one.