Скачать или смотреть Capturing, validating and publishing data to the GUDID. The Easy Way

Have you heard the latest FDA advice...?

“FDA’s experience and feedback from industry indicate that device labellers often take a number of actions to organize, collect and validate data—before they get a GUDID account or submit device identifier (DI) records. We strongly encourage all device labellers to take such actions to ensure their readiness to meet UDI requirements and streamline the GUDID submission process.”

At LANSA we have developed an online, easy-to-use service that enables you to efficiently organise, validate and publish your UDI data to the GUDID without having to learn the intricacies of the FDA rule or risk getting it wrong.

But…. It’s not just about the FDA rule...

Our low-cost, subscription service also prepares you for future product data requirements from other trading partners and regulatory entities, like:

The UK Department of Health's eProcurement Strategy
European Commission - EUDAMED –UDI Initiative
GS1 Global Data Synchronization Network (GDSN) participation