How Device And Diagnostic Teams Run Compliant Studies Without Enterprise EDC Overhead

By Kevin Thornton, Director of Marketing

Medical device, diagnostic, and IVD teams running low-complexity studies face a persistent structural problem: enterprise EDC systems bring cost and build time the work doesn't justify, while spreadsheets leave nothing usable for an auditor. The gap is real, and most teams either overbuy or accept compliance risk.

In this 30-minute product spotlight, Castor's Chief Product Officer Lisa Charlton and Senior Solutions Consultant Angie Martinez present a third option and construct a compliant study live, without code, to show how a device team moves from protocol to audit-ready data capture in weeks. The session also addresses where that starting point leads as programs expand toward post-market evidence requirements. Watch the webinar to see the approach in practice.