UDI & MDR Resources for Medical Device Makers

UDI and FDA’s New QMSR Inspection Process

FDA’s QMSR inspection process is live. Learn how UDI will be inspected under CP 7382.850 and how USDM helps manufacturers prepare and comply.

Jay Crowley
- February 5, 2026

Blogs

Medical Device

Quality Assurance

EUDAMED Has Landed – What It Means for You, Now

On-Demand: Discover what the EUDAMED launch means for MDR/IVDR compliance—and how to stay audit-ready with USDM’s expert guidance. Watch now.

On Demand, Webinars

Medical Device

Regulatory

UDI Compliance and the Future of Medical Device Data

EUDAMED is here—avoid costly UDI compliance mistakes. Discover how to ensure data integrity, achieve compliance, and protect market access for medical devices.

Jay Crowley
- August 11, 2025

Blogs

Medical Device

Information Technology, Manufacturing, Quality Assurance, Regulatory

Join USDM at RAPS Convergence 2025

Join USDM and BYRD Health at RAPS Convergence 2025 to explore EUDAMED compliance, UDI strategies, and MDR/IVDR readiness. Visit booth #537 or register for our workshop.