RAPS preconference workshop

Global UDI Compliance and Registration Strategies

Register for USDM’s RAPS Convergence 2026 preconference workshop on global UDI compliance, EUDAMED submissions, device registration, and global UDI deadlines.

Register for the workshop View RAPS sponsor page
UDI registration and EUDAMED submission visual for global medical device regulatory compliance.

Register for the RAPS preconference UDI workshop.

Join USDM for Global UDI Compliance and Registration Strategies, a focused preconference workshop for medical device teams preparing for EUDAMED UDI and Device Registration submissions while aligning with global UDI initiatives.

The session is designed for regulatory, quality, labeling, master data, and medical device operations teams that need a practical way to manage deadlines, data quality, submission readiness, and cross-market requirements.

Preconference workshop

Global UDI Compliance and Registration Strategies

Learn how to streamline your EUDAMED UDI and Device Registration submissions and align with global UDI initiatives.

This workshop will cover global UDI compliance activity with a focus on:

  • Manufacturers have about two months before the 27 November 2026 deadline for EUDAMED device registration and UDI database submissions.
  • The EUDAMED deadline for contact lenses, including use of the Master UDI-DI, is also upcoming on 9 November 2026.
  • The 31 December 2026 Swissdamed deadline.
  • FDA QMSR inspection technique updates and FDA activity around GUDID data quality.
  • Australia TGA UDI implementation, including the first 1 July 2026 deadline for non-EU certified devices that has already passed.

Live EUDAMED syndication demonstration

BYRD Health will present a live demonstration of its EUDAMED Syndication Solutions, showing how teams can support submission activity with stronger data flow, governance, and operational control.

Register for the preconference workshop

Use this form to register for Global UDI Compliance and Registration Strategies on September 15 from 1:00-3:00 PM at the JW Marriott in Charlotte.

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About the workshop hosts

USDM helps medical device manufacturers build practical UDI, EU MDR, EUDAMED, GUDID, and regulatory data programs that connect strategy, data readiness, submission execution, and inspection-ready evidence.

BYRD Health will present a live EUDAMED Syndication Solutions demonstration as part of the workshop.