Unique Device Identifica​tion (UDI) for Postmarket Surveilla

[admin]

The FDA is holding a public workshop on the adoption, implementation, and use of unique device identifiers (UDIs) in various health-related electronic data systems. The purpose of this workshop is to engage multiple stakeholders to obtain information and comments on issues confronting the effective and efficient incorporation of UDIs into appropriate data sets, to identify barriers and incentives to their adoption and use, and to understand the best solutions and practices to resolve open issues.
Go to http://www.fda.gov/MedicalDevices/NewsE ... 263947.htm for more information.