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.
The GUDID FAQ eBook for Compliance
Today, Medical Device manufacturers are staring down the barrel of a number of critical compliance deadlines specific to GUDID (Global Unique Device Identification Database). Having the right processes and systems can simplify this journey substantially.
This eBook is intended to serve as a reference tool and mini-guidebook as your team navigates the complexities of GUDID.