Achieving EU MDR / IVDR Compliance with Inspirage and Oracle

Is your organization on track to comply with the EU MDR / IVDR regulations by the deadline?

Join us on Jan 16th to learn how your organization can achieve European Union Medical Device Regulation (EU MDR) and In Vitro Diagnostic Regulation (IVDR) compliance. Learn what pitfalls to avoid to minimize disruption to business processes on the path to EU MDR / IVDR compliance and ways to help your company transition smoothly and comply with the new regulations.

Transition phases are always a challenge. EU MDR / IVDR regulation compliance requires time, investment, and a thorough understanding of the technological landscape of the organization’s processes.