Transforming Device Identification: UNIQUE DEVICE IDENTIFICATION (UDI)

March 10, 2020 10:00–11:00 Eastern Time (US & Canada)

In 2013 the US FDA published a regulation establishing UDI as a manufacturer requirement for identifying a medical device. This webinar will provide an overview of those requirements and then discuss the role UDI is playing to improve device tracking, adverse event reporting, recall management, and medical device registry work to support clinical evidence development. Th importance of cross-stakeholder engagement to advance UDI adoption In electronic health information will also be discussed.

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