UDI Reference Center
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Global UDI Reference Center
Global UDI Developments
There is ongoing uncertainty when it comes to Unique Device Identifcation (UDI) regulations and compliance timelines as each country’s regulator continues to change the scope of their UDI implementation. Despite the concerted efforts of International Medical Device Regulators Forum (IMDRF), divergence in UDI policy and strategy is adding complexity for medical device companies to comply with regulatory data submission mandates, especially those with multi-national operations. Fortunately, Innovit is here to to help you navigate these country-specific deadlines and UDI data requirements.
Top 12 Things to Prepare for Your UDI Journey
All manufacturers who distribute their products multi-nationally must address the rapidly approaching global UDI requirements, which not only apply in the U.S. and Europe, but are also underway in China, South Korea, Saudi Arabia, and more. In addition, several countries are in various stages of developing their UDI requirements, and it’s only a matter of time before UDI will be required everywhere.
Download our guide to learn the top 12 steps to take on your journey toward global UDI compliance.