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Democratizing MDM

Democratizing MDM

In a global, data-driven and digital world, standardizing, mastering and leveraging high volumes of master data in an automated process is a strategic and business imperative.

Key Insights from Early EUDAMED Testing

Key Insights from Early EUDAMED Testing

Key Insights from Early EUDAMED Testing & Post Go-Live Feedback Webinar   Lorem ipsum dolor sit amet, consectetur adipiscing elit. Fusce volutpat rhoncus consectetur. Proin sed blandit arcu. Duis scelerisque justo sit amet dui posuere...

Innovit & 1WorldSync: “The Arthrex Journey”

Innovit & 1WorldSync: “The Arthrex Journey”

Innovit & 1WorldSync: "The Arthrex Journey” Achieving Data Requirements for UDI   Innovit and 1WorldSync experts discuss the Arthrex Journey” Achieving Data Requirements for UDI & Beyond and the delivery of a PIM Lite solution.

How to meet the Growing Challenges

How to meet the Growing Challenges

Seven years ago when the Federal Drug Administration (FDA) announced its Unique Device Identification (UDI) regulations, there were no off-the-shelf solutions for submitting regulatory data to the Global UDI Database (GUDID).