Customer-Exclusive Webinars

osapiens HUB for Medical Devices

October 1, 2026, 14:00

Many osapiens customers in the medical device industry currently rely on BYRD to manage UDI and product data compliance across EUDAMED, GUDID, TGA, Swissdamed, and other regulatory databases.

As part of the continued evolution of our Medical Devices offering, osapiens is transitioning these capabilities to the osapiens HUB for Medical Devices, providing customers with a modern, scalable platform for managing their regulatory data and submission processes.

Customers currently using BYRD are encouraged to start preparing for this transition and understand what it means for their existing processes, integrations, and regulatory submissions.

This session is designed for teams who want to understand what is changing, the benefits of the osapiens HUB for Medical Devices, and how to prepare for a smooth transition while maintaining continuity of their ongoing regulatory compliance activities.

What you'll learn:

  1. Why osapiens is transitioning Medical Devices capabilities from BYRD to the osapiens HUB
  2. What is changing and the key capabilities of the osapiens HUB for Medical Devices
  3. The migration approach, timeline, and what customers can expect at each stage
  4. How to prepare your organization, integrations, processes, and data for a smooth transition

Language: EN

Register now