At the 2014 UDI Conference, FDA commented on their plans to share Unique Device Identification (UDI) data from the Global UDI Database (GUDID) with healthcare providers and the public. Approximately 33,000 records have been uploaded to the GUDID and once a meaningful set of data records are established (anticipated in Jan 2015), they will share through the National Library of Medicine (NLM) website where pharmaceutical label information is currently stored.
USDM Life Sciences will help you assess, plan and execute the changes and enhancements necessary to meet regulatory requirements, including the Drug Supply Chain Security Act, Unique Device Identification and Meaningful Use Rule.
How do you plan to use this data? Email us your ideas.
**The world's largest biomedical library, the National Library of Medicine maintains and makes available a vast print collection and produces electronic information resources on a wide range of topics that are searched billions of times each year by millions of people around the globe. It also supports and conducts research, development and training in biomedical informatics and health information technology.
USDM Life Sciences offers healthcare a comprehensive assessment, strategy and solutions to implement end to end traceability of pharmaceutical and medical devices from point of receipt through to the electronic health record.