We are pleased to be both sponsor and speaker at the Global UDI & Master Data Forum, which will take place as online event.

Besides various speakers, for example FDA, GMDN and GS1, our co-founder Patrick Pfau will give insights on “How to master the global UDI Challenge” on the basis of a real world example. Thereby he will discuss the strategic considerations that need to be made before establishing a global UDI setup as well as the importance of a flexible framework capable of handling multiple agencies. In addition, he will explain how the phases of multiple UDI projects merge into an ongoing UDI program cycle based on current UDI projects for FDA GUDID and EC EUDAMED.

Covering the requirements and standards of different regulatory authorities worldwide in order to ensure global UDI compliance is a key challenge for medical device manufacturers, especially because they have to keep track of unclear timelines for upcoming requirements and their tight deadlines. The Global UDI & Master Data Forum is the industries leading platform for answers regarding global UDI compliance and effective master data management by bringing together all key stakeholders – from healthcare providers, notified bodies and medical device manufacturers.

Register here for the Global UDI & Master Data Forum and join Patrick Pfau’s talk on Conference Day 2, November 12, 2020.

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