Ortho-Clinical Diagnostics, Eucomed UDI Task Force, GS1 Global and Endologix discuss the European UDI landscape for medical devices.
As the medical device industry awaits the finalised regulations from the EU, some have looked at the FDA and predicted that the EU is likely to mirror the preferences of the US body.
In this exclusive eBook, three UDI experts discuss the European landscape for medical devices. The interview panel is made up of Andrew Rutter, Senior Regulatory Affairs Associate for Ortho-Clinical Diagnostics and Chair of the Eucomed UDI Task Force, Geraldine Lissalde-Bonnet, Senior Public Policy Manager for Healthcare at GS1 Global Office, and Dawn Fowler, Senior Manager for Global Labeling / Training at Endologix. The piece explores:
How affected parties can thrive within the current UDI changes
The EU's position on UDIs for medical devices
Updates on the regulatory position on direct marking
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