Veeva Safety supports linking a secondary, device-specific agency to a Country. New Product Registrations for that country automatically inherit the agency. This ensures that for medical devices registered in a specific country, Vault correctly runs device agency reporting rules (EUDAMED in the EU for example) rather than defaulting to medicinal product logic.
Once you have configured this feature, see Manage Organizations and Manage Products for more information.
Update Object Layouts
To configure this feature, add the Device Agency field to the Country and Product Registration object layouts.