October 7-9, 2025 | Pittsburgh, PA
RAPS Convergence is the largest annual gathering of global regulatory affairs professionals, where regulators, manufacturers, and compliance leaders come together to tackle the future of global health product regulation. USDM Life Sciences is proud to return with BYRD Health, an osapiens company, to lead essential sessions on navigating the evolving EUDAMED landscape.
Find us at Booth #537
Why Attend
With Europe’s new EUDAMED deployment timeline now official, and the critical medical device data entry required in 2026, there’s never been a more critical time to align your global regulatory strategy. RAPS Convergence gives you direct access to:
- Experts from leading notified bodies, regulatory consultancies, and software providers
- Workshops and live demos to guide MDR and IVDR readiness
- Timely discussions on UDI, PMS, and Vigilance requirements
- A powerful network of regulatory professionals and compliance strategists
Whether you’re managing global submissions or local syndication challenges, this conference offers actionable insights to help your teams get ahead.
Pre-Conference Workshop
At RAPS 2025, USDM is partnering with BYRD Health to deliver a must-attend workshop focused on EUDAMED implementation, syndication, and regulatory transformation.
📅 Tuesday, October 7th | 🕞 2:00 PM – 4:00 PM | 📍 The Westin Pittsburgh
USDM’s Jay Crowley and BYRD Health’s Jeff Holzman will present a live demonstration of EUDAMED Syndication Solutions, walking you through product data harmonization and regulatory timelines. This complimentary, invite-only session includes lunch and a detailed walkthrough of the 2026 mandatory UDI enforcement deadline. Learn how to streamline your UDI and Device Registration module submissions and align with global UDI initiatives.
👉 Registration is required. Fill out the form to register for the pre-conference workshop.
Let’s Talk UDI, MDR, IVDR, and Syndication
Visit booth #537 to discuss:
- Strategies for meeting EU MDR/IVDR deadlines
- EUDAMED product data submission and system integration
- Vigilance & post-market surveillance best practices
- Global UDI alignment and multi-region syndication tools
As regulators evolve their systems, USDM ensures your processes and technologies stay compliant and future-ready.
Connect with the Leaders in Regulatory Innovation
Join USDM and BYRD Health in Pittsburgh to ensure you’re not only compliant—but confident in your global regulatory approach.
About the USDM Life Sciences and BYRD Health partnership.
About BYRD Health, an osapiens company
The Platform for Product Data Management and Syndication
The osapiens platform provides efficiency, flexibility, ease of use and superb integration capabilities for Medical Device companies of all sizes. With osapiens for Medical Device you can manage and syndicate Product Master Data (GUDID, EUDAMED, GDSN, etc.) satisfying your regulatory and commercial Product Master Data Management and Syndication needs. We provide the optimal solution(s) for companies of all sizes all in a pre-FDA validated environment with USDM Cloud assurance.